Linked Data
ClinVar Variation Id:
531847
dbSNP Id:
rs368995503
ExAC:
9:140638512 G / C
gnomAD v2:
9-140638512-G-C
gnomAD v3:
9-137744060-G-C
gnomAD v4:
9-137744060-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.137744060G>C , CM000671.2:g.137744060G>C | GRCh38 |
| NC_000009.11:g.140638512G>C , CM000671.1:g.140638512G>C | GRCh37 |
| NC_000009.10:g.139758333G>C | NCBI36 |
| NG_011776.1:g.130069G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000460843.6:c.1140G>C MANE Select | ENSP00000417980.1:p.Glu380Asp | |
| ENST00000629335.2:c.1140G>C | ENSP00000490056.1:p.Glu380Asp | |
| ENST00000636027.1:c.1026G>C | ENSP00000489961.1:p.Glu342Asp | |
| ENST00000637161.1:c.1047G>C | ENSP00000490328.1:p.Glu349Asp | |
| ENST00000637261.1:c.1180G>C | ENSP00000490815.1:n.1180G>C | |
| ENST00000637318.1:c.264G>C | ENSP00000490611.1:p.Glu88Asp | |
| ENST00000637977.1:c.1085G>C | ||
| ENST00000638071.1:c.845G>C | ||
| ENST00000640639.1:c.309G>C | ENSP00000491823.1:p.Glu103Asp | |
| ENST00000371394.6:c.*875G>C | ENSP00000485945.1:n.*875G>C | |
| ENST00000460843.5:c.1140G>C | ENSP00000417980.1:p.Glu380Asp | |
| ENST00000462484.5:c.1140G>C | ENSP00000417328.1:p.Glu380Asp | |
| ENST00000478940.1:n.431G>C | ||
| ENST00000495657.5:n.490G>C | ||
| ENST00000626066.2:c.1043G>C | ||
| ENST00000629808.2:c.311G>C | ||
| NM_001145527.1:c.1140G>C | NP_001138999.1:p.Glu380Asp | |
| NM_024757.4:c.1140G>C | NP_079033.4:p.Glu380Asp | |
| XM_005266105.3:c.1131G>C | XP_005266162.1:p.Glu377Asp | |
| XM_005266110.1:c.1047G>C | XP_005266167.1:p.Glu349Asp | |
| XM_006717288.2:c.1122G>C | XP_006717351.1:p.Glu374Asp | |
| XM_011519021.1:c.1149G>C | XP_011517323.1:p.Glu383Asp | |
| XM_011519022.1:c.1146G>C | XP_011517324.1:p.Glu382Asp | |
| XM_011519023.1:c.1128G>C | XP_011517325.1:p.Glu376Asp | |
| XM_011519024.1:c.1149G>C | XP_011517326.1:p.Glu383Asp | |
| XM_011519025.1:c.1047G>C | XP_011517327.1:p.Glu349Asp | |
| XM_011519026.1:c.1149G>C | XP_011517328.1:p.Glu383Asp | |
| XM_011519027.1:c.1149G>C | XP_011517329.1:p.Glu383Asp | |
| XM_011519028.1:c.1149G>C | XP_011517330.1:p.Glu383Asp | |
| XM_011519033.1:c.1128G>C | XP_011517335.1:p.Glu376Asp | |
| NM_001354259.1:c.1047G>C | NP_001341188.1:p.Glu349Asp | |
| NM_001354263.1:c.1119G>C | NP_001341192.1:p.Glu373Asp | |
| NM_001354611.1:c.1140G>C | NP_001341540.1:p.Glu380Asp | |
| NM_001354612.1:c.1047G>C | NP_001341541.1:p.Glu349Asp | |
| XM_005266105.5:c.1131G>C | XP_005266162.1:p.Glu377Asp | |
| XM_011519021.3:c.1149G>C | XP_011517323.1:p.Glu383Asp | |
| XM_011519022.3:c.1146G>C | XP_011517324.1:p.Glu382Asp | |
| XM_011519023.3:c.1128G>C | XP_011517325.1:p.Glu376Asp | |
| XM_017015134.1:c.1125G>C | XP_016870623.1:p.Glu375Asp | |
| XM_017015136.2:c.1119G>C | XP_016870625.1:p.Glu373Asp | |
| XM_017015137.1:c.1026G>C | XP_016870626.1:p.Glu342Asp | |
| XM_017015138.1:c.1026G>C | XP_016870627.1:p.Glu342Asp | |
| XM_024447674.1:c.1047G>C | XP_024303442.1:p.Glu349Asp | |
| XM_024447675.1:c.1047G>C | XP_024303443.1:p.Glu349Asp | |
| XM_024447676.1:c.264G>C | XP_024303444.1:p.Glu88Asp | |
| XM_024447677.1:c.264G>C | XP_024303445.1:p.Glu88Asp | |
| XM_024447678.1:c.1047G>C | XP_024303446.1:p.Glu349Asp | |
| XM_024447679.1:c.1047G>C | XP_024303447.1:p.Glu349Asp | |
| XM_024447680.1:c.1026G>C | XP_024303448.1:p.Glu342Asp | |
| NM_024757.5:c.1140G>C MANE Select | NP_079033.4:p.Glu380Asp | |
| NM_001145527.2:c.1140G>C | NP_001138999.1:p.Glu380Asp | |
| NM_001354259.2:c.1047G>C | NP_001341188.1:p.Glu349Asp | |
| NM_001354263.2:c.1119G>C | NP_001341192.1:p.Glu373Asp | |
| NM_001354611.2:c.1140G>C | NP_001341540.1:p.Glu380Asp | |
| NM_001354612.2:c.1047G>C | NP_001341541.1:p.Glu349Asp |