Linked Data
ClinVar Variation Id:
289845
dbSNP Id:
rs376439815
ExAC:
5:88018511 G / A
gnomAD v2:
5-88018511-G-A
gnomAD v3:
5-88722694-G-A
gnomAD v4:
5-88722694-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.88722694G>A , CM000667.2:g.88722694G>A | GRCh38 |
| NC_000005.9:g.88018511G>A , CM000667.1:g.88018511G>A | GRCh37 |
| NC_000005.8:g.88054267G>A | NCBI36 |
| NG_023427.1:g.186412C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000707127.1:c.954C>T (MEF2C) | ENSP00000516755.1:p.His318= | |
| ENST00000503554.4:c.894C>T (MEF2C) | ENSP00000487437.2:p.His298= | |
| ENST00000504921.7:c.1332C>T (MEF2C) MANE Select | ENSP00000421925.5:p.His444= | |
| ENST00000636143.1:n.1173C>T (MEF2C) | ||
| ENST00000636294.1:c.1332C>T (MEF2C) | ENSP00000490473.1:p.His444= | |
| ENST00000636998.1:c.1236C>T (MEF2C) | ENSP00000490630.1:p.His412= | |
| ENST00000637481.1:c.1299C>T (MEF2C) | ENSP00000490354.1:p.His433= | |
| ENST00000637732.1:c.1236C>T (MEF2C) | ENSP00000490241.1:p.His412= | |
| ENST00000340208.9:c.1362C>T (MEF2C) | ENSP00000340874.5:p.His454= | |
| ENST00000424173.6:c.1302C>T (MEF2C) | ENSP00000389610.2:p.His434= | |
| ENST00000437473.6:c.1332C>T (MEF2C) | ENSP00000396219.2:p.His444= | |
| ENST00000504921.6:c.1332C>T (MEF2C) | ENSP00000421925.4:p.His444= | |
| ENST00000506554.5:c.*59C>T (MEF2C) | ENSP00000425636.1:n.*59C>T | |
| ENST00000508569.5:c.1308C>T (MEF2C) | ENSP00000423597.2:p.His436= | |
| ENST00000510942.5:c.1212C>T (MEF2C) | ENSP00000422390.2:p.His404= | |
| ENST00000514015.5:c.1236C>T (MEF2C) | ENSP00000424606.1:p.His412= | |
| ENST00000514028.5:c.1236C>T (MEF2C) | ENSP00000426665.2:p.His412= | |
| ENST00000625585.2:c.1326C>T (MEF2C) | ENSP00000487538.1:p.His442= | |
| ENST00000625674.2:c.1302C>T (MEF2C) | ENSP00000487430.1:p.His434= | |
| ENST00000626391.2:c.1092C>T (MEF2C) | ENSP00000487184.1:p.His364= | |
| ENST00000627170.2:c.523C>T (MEF2C) | ENSP00000487157.1:n.523C>T | |
| ENST00000627659.2:c.1206C>T (MEF2C) | ENSP00000486490.1:p.His402= | |
| ENST00000627717.2:c.619C>T (MEF2C) | ENSP00000486932.1:n.619C>T | |
| ENST00000628656.2:c.1164C>T (MEF2C) | ENSP00000487311.1:p.His388= | |
| ENST00000629612.2:c.1308C>T (MEF2C) | ENSP00000486554.1:p.His436= | |
| NM_001131005.2:c.1302C>T (MEF2C) | NP_001124477.1:p.His434= | |
| NM_001193347.1:c.1362C>T (MEF2C) | NP_001180276.1:p.His454= | |
| NM_001193348.1:c.1164C>T (MEF2C) | NP_001180277.1:p.His388= | |
| NM_001193349.1:c.1092C>T (MEF2C) | NP_001180278.1:p.His364= | |
| NM_001193350.1:c.1332C>T (MEF2C) | NP_001180279.1:p.His444= | |
| NM_001308002.1:c.1308C>T (MEF2C) | NP_001294931.1:p.His436= | |
| NM_002397.4:c.1332C>T (MEF2C) | NP_002388.2:p.His444= | |
| XM_005248511.1:c.1332C>T (MEF2C) | XP_005248568.1:p.His444= | |
| XM_006714618.1:c.1332C>T (MEF2C) | XP_006714681.1:p.His444= | |
| XM_006714619.1:c.1332C>T (MEF2C) | XP_006714682.1:p.His444= | |
| XM_006714625.2:c.1362C>T (MEF2C) | XP_006714688.1:p.His454= | |
| XM_011543396.1:c.1332C>T (MEF2C) | XP_011541698.1:p.His444= | |
| XM_011543397.1:c.1326C>T (MEF2C) | XP_011541699.1:p.His442= | |
| XM_011543399.1:c.1302C>T (MEF2C) | XP_011541701.1:p.His434= | |
| XM_011543400.1:c.1236C>T (MEF2C) | XP_011541702.1:p.His412= | |
| XM_011543401.1:c.1212C>T (MEF2C) | XP_011541703.1:p.His404= | |
| XM_011543402.1:c.1206C>T (MEF2C) | XP_011541704.1:p.His402= | |
| XM_011543403.1:c.1188C>T (MEF2C) | XP_011541705.1:p.His396= | |
| XM_011543404.1:c.1164C>T (MEF2C) | XP_011541706.1:p.His388= | |
| XM_011543405.1:c.1092C>T (MEF2C) | XP_011541707.1:p.His364= | |
| NM_001193349.2:c.1092C>T (MEF2C) | NP_001180278.1:p.His364= | |
| NM_001308002.2:c.1308C>T (MEF2C) | NP_001294931.1:p.His436= | |
| NM_001363581.1:c.1236C>T (MEF2C) | NP_001350510.1:p.His412= | |
| NM_001364329.1:c.1332C>T (MEF2C) | NP_001351258.1:p.His444= | |
| NM_001364330.1:c.1332C>T (MEF2C) | NP_001351259.1:p.His444= | |
| NM_001364331.1:c.1332C>T (MEF2C) | NP_001351260.1:p.His444= | |
| NM_001364332.1:c.1092C>T (MEF2C) | NP_001351261.1:p.His364= | |
| NM_001364333.1:c.1308C>T (MEF2C) | NP_001351262.1:p.His436= | |
| NM_001364334.1:c.1236C>T (MEF2C) | NP_001351263.1:p.His412= | |
| NM_001364335.1:c.1236C>T (MEF2C) | NP_001351264.1:p.His412= | |
| NM_001364336.1:c.1236C>T (MEF2C) | NP_001351265.1:p.His412= | |
| NM_001364337.1:c.1236C>T (MEF2C) | NP_001351266.1:p.His412= | |
| NM_001364338.1:c.1266C>T (MEF2C) | NP_001351267.1:p.His422= | |
| NM_001364339.1:c.1212C>T (MEF2C) | NP_001351268.1:p.His404= | |
| NM_001364340.1:c.1212C>T (MEF2C) | NP_001351269.1:p.His404= | |
| NM_001364341.1:c.1212C>T (MEF2C) | NP_001351270.1:p.His404= | |
| NM_001364342.1:c.1212C>T (MEF2C) | NP_001351271.1:p.His404= | |
| NM_001364343.1:c.1206C>T (MEF2C) | NP_001351272.1:p.His402= | |
| NM_001364344.1:c.1188C>T (MEF2C) | NP_001351273.1:p.His396= | |
| NM_001364345.1:c.*67C>T (MEF2C) | NP_001351274.1:n.*67C>T | |
| NM_001364346.1:c.*67C>T (MEF2C) | NP_001351275.1:n.*67C>T | |
| NM_001364347.1:c.*67C>T (MEF2C) | NP_001351276.1:n.*67C>T | |
| NM_001364348.1:c.*67C>T (MEF2C) | NP_001351277.1:n.*67C>T | |
| NM_001364349.1:c.*67C>T (MEF2C) | NP_001351278.1:n.*67C>T | |
| NM_001364350.1:c.*67C>T (MEF2C) | NP_001351279.1:n.*67C>T | |
| NM_001364352.1:c.*67C>T (MEF2C) | NP_001351281.1:n.*67C>T | |
| NM_001364353.1:c.954C>T (MEF2C) | NP_001351282.1:p.His318= | |
| NM_001364354.1:c.*67C>T (MEF2C) | NP_001351283.1:n.*67C>T | |
| NM_001364355.1:c.*67C>T (MEF2C) | NP_001351284.1:n.*67C>T | |
| NM_001364356.1:c.858C>T (MEF2C) | NP_001351285.1:p.His286= | |
| NM_001364357.1:c.786C>T (MEF2C) | NP_001351286.1:p.His262= | |
| NR_146284.1:n.326G>A (MEF2C-AS2) | ||
| XM_005248511.3:c.1332C>T (MEF2C) | XP_005248568.1:p.His444= | |
| XM_006714625.4:c.1362C>T (MEF2C) | XP_006714688.1:p.His454= | |
| XM_011543396.3:c.1332C>T (MEF2C) | XP_011541698.1:p.His444= | |
| XM_011543397.3:c.1326C>T (MEF2C) | XP_011541699.1:p.His442= | |
| XM_017009475.2:c.1326C>T (MEF2C) | XP_016864964.1:p.His442= | |
| XM_017009478.2:c.1302C>T (MEF2C) | XP_016864967.1:p.His434= | |
| XM_024446055.1:c.1332C>T (MEF2C) | XP_024301823.1:p.His444= | |
| XM_024446056.1:c.1332C>T (MEF2C) | XP_024301824.1:p.His444= | |
| XM_024446057.1:c.1326C>T (MEF2C) | XP_024301825.1:p.His442= | |
| XM_024446058.1:c.1326C>T (MEF2C) | XP_024301826.1:p.His442= | |
| XM_024446059.1:c.1326C>T (MEF2C) | XP_024301827.1:p.His442= | |
| NM_001193350.2:c.1332C>T (MEF2C) | NP_001180279.1:p.His444= | |
| NM_001308002.3:c.1308C>T (MEF2C) | NP_001294931.1:p.His436= | |
| NM_001364329.2:c.1332C>T (MEF2C) | NP_001351258.1:p.His444= | |
| NM_001364330.2:c.1332C>T (MEF2C) | NP_001351259.1:p.His444= | |
| NM_001364331.2:c.1332C>T (MEF2C) | NP_001351260.1:p.His444= | |
| NM_001364333.2:c.1308C>T (MEF2C) | NP_001351262.1:p.His436= | |
| NM_001364339.2:c.1212C>T (MEF2C) | NP_001351268.1:p.His404= | |
| NM_001364344.2:c.1188C>T (MEF2C) | NP_001351273.1:p.His396= | |
| NM_001364345.2:c.*67C>T (MEF2C) | NP_001351274.1:n.*67C>T | |
| NM_001364346.2:c.*67C>T (MEF2C) | NP_001351275.1:n.*67C>T | |
| NM_001364347.2:c.*67C>T (MEF2C) | NP_001351276.1:n.*67C>T | |
| NM_001364348.2:c.*67C>T (MEF2C) | NP_001351277.1:n.*67C>T | |
| NM_001364349.2:c.*67C>T (MEF2C) | NP_001351278.1:n.*67C>T | |
| NM_001364352.2:c.*67C>T (MEF2C) | NP_001351281.1:n.*67C>T | |
| NM_001364353.2:c.954C>T (MEF2C) | NP_001351282.1:p.His318= | |
| NM_001364354.2:c.*67C>T (MEF2C) | NP_001351283.1:n.*67C>T | |
| NM_001364355.2:c.*67C>T (MEF2C) | NP_001351284.1:n.*67C>T | |
| NM_002397.5:c.1332C>T (MEF2C) MANE Select | NP_002388.2:p.His444= | |
| NM_001193349.3:c.1092C>T (MEF2C) | NP_001180278.1:p.His364= | |
| NM_001363581.2:c.1236C>T (MEF2C) | NP_001350510.1:p.His412= | |
| NM_001364332.2:c.1092C>T (MEF2C) | NP_001351261.1:p.His364= | |
| NM_001364334.2:c.1236C>T (MEF2C) | NP_001351263.1:p.His412= | |
| NM_001364335.2:c.1236C>T (MEF2C) | NP_001351264.1:p.His412= | |
| NM_001364336.2:c.1236C>T (MEF2C) | NP_001351265.1:p.His412= | |
| NM_001364337.2:c.1236C>T (MEF2C) | NP_001351266.1:p.His412= | |
| NM_001364338.2:c.1266C>T (MEF2C) | NP_001351267.1:p.His422= | |
| NM_001364340.2:c.1212C>T (MEF2C) | NP_001351269.1:p.His404= | |
| NM_001364341.2:c.1212C>T (MEF2C) | NP_001351270.1:p.His404= | |
| NM_001364342.2:c.1212C>T (MEF2C) | NP_001351271.1:p.His404= | |
| NM_001364343.2:c.1206C>T (MEF2C) | NP_001351272.1:p.His402= | |
| NM_001364350.2:c.*67C>T (MEF2C) | NP_001351279.1:n.*67C>T | |
| NM_001364356.2:c.858C>T (MEF2C) | NP_001351285.1:p.His286= | |
| NM_001364357.2:c.786C>T (MEF2C) | NP_001351286.1:p.His262= |