Linked Data
ClinVar Variation Id:
143750
dbSNP Id:
rs61751446
ExAC:
X:153296337 G / A
gnomAD v2:
X-153296337-G-A
gnomAD v3:
X-154030886-G-A
gnomAD v4:
X-154030886-G-A
COSMIC:
COSM5367342
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154030886G>A , CM000685.2:g.154030886G>A | GRCh38 |
| NC_000023.10:g.153296337G>A , CM000685.1:g.153296337G>A | GRCh37 |
| NC_000023.9:g.152949531G>A | NCBI36 |
| NG_007107.2:g.111242C>T | |
| NG_007107.3:g.111218C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000303391.11:c.942C>T MANE Plus Clinical | ENSP00000301948.6:p.Ile314= | |
| ENST00000453960.7:c.978C>T MANE Select | ENSP00000395535.2:p.Ile326= | |
| ENST00000637917.1:c.116C>T | ||
| ENST00000303391.10:c.942C>T | ENSP00000301948.6:p.Ile314= | |
| ENST00000407218.5:c.*314C>T | ENSP00000384865.2:n.*314C>T | |
| ENST00000453960.6:c.978C>T | ENSP00000395535.2:p.Ile326= | |
| ENST00000619732.4:c.942C>T | ENSP00000480973.1:p.Ile314= | |
| ENST00000622433.4:c.928C>T | ENSP00000484470.1:p.Arg310Ter | |
| ENST00000628176.2:c.*314C>T | ENSP00000486978.1:n.*314C>T | |
| NM_001110792.1:c.978C>T | NP_001104262.1:p.Ile326= | |
| NM_001316337.1:c.663C>T | NP_001303266.1:p.Ile221= | |
| NM_004992.3:c.942C>T | NP_004983.1:p.Ile314= | |
| XM_005274681.3:c.942C>T | XP_005274738.1:p.Ile314= | |
| XM_005274682.3:c.663C>T | XP_005274739.1:p.Ile221= | |
| XM_005274683.3:c.663C>T | XP_005274740.1:p.Ile221= | |
| XM_006724819.2:c.273C>T | XP_006724882.1:p.Ile91= | |
| XM_011531166.1:c.663C>T | XP_011529468.1:p.Ile221= | |
| XM_006724819.3:c.273C>T | XP_006724882.1:p.Ile91= | |
| XM_011531166.2:c.663C>T | XP_011529468.1:p.Ile221= | |
| XM_024452383.1:c.663C>T | XP_024308151.1:p.Ile221= | |
| XM_024452384.1:c.663C>T | XP_024308152.1:p.Ile221= | |
| NM_001110792.2:c.978C>T MANE Select | NP_001104262.1:p.Ile326= | |
| NM_001316337.2:c.663C>T | NP_001303266.1:p.Ile221= | |
| NM_001369391.2:c.663C>T | NP_001356320.1:p.Ile221= | |
| NM_001369392.2:c.663C>T | NP_001356321.1:p.Ile221= | |
| NM_001369393.2:c.663C>T | NP_001356322.1:p.Ile221= | |
| NM_001369394.1:c.663C>T | NP_001356323.1:p.Ile221= | |
| NM_001369394.2:c.663C>T | NP_001356323.1:p.Ile221= | |
| NM_001386137.1:c.273C>T | NP_001373066.1:p.Ile91= | |
| NM_001386138.1:c.273C>T | NP_001373067.1:p.Ile91= | |
| NM_001386139.1:c.273C>T | NP_001373068.1:p.Ile91= | |
| NM_004992.4:c.942C>T MANE Plus Clinical | NP_004983.1:p.Ile314= |