Linked Data
ClinVar Variation Id:
3074876
ClinVar RCV Id:
RCV004015402
gnomAD v4:
13-51941156-T-C
COSMIC:
COSM1660696
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.51941156T>C , CM000675.2:g.51941156T>C | GRCh38 |
| NC_000013.10:g.52515292T>C , CM000675.1:g.52515292T>C | GRCh37 |
| NC_000013.9:g.51413293T>C | NCBI36 |
| NG_008806.1:g.75339A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000634296.2:c.*1131A>G | ENSP00000489512.2:n.*1131A>G | |
| ENST00000673864.2:c.*2225A>G | ENSP00000501045.2:n.*2225A>G | |
| ENST00000674147.2:c.2860A>G | ENSP00000500964.2:p.Ile954Val | |
| ENST00000242839.10:c.3481A>G MANE Select | ENSP00000242839.5:p.Ile1161Val | |
| ENST00000344297.9:c.2860A>G | ENSP00000342559.5:p.Ile954Val | |
| ENST00000400366.6:c.3148A>G | ENSP00000383217.3:p.Ile1050Val | |
| ENST00000448424.7:c.3229A>G | ENSP00000416738.3:p.Ile1077Val | |
| ENST00000673772.1:c.3247A>G | ENSP00000501168.1:p.Ile1083Val | |
| ENST00000673867.1:n.3620A>G | ||
| ENST00000674126.1:n.3844A>G | ||
| ENST00000674147.1:c.2416A>G | ENSP00000500964.1:p.Ile806Val | |
| ENST00000242839.8:c.3481A>G | ENSP00000242839.4:p.Ile1161Val | |
| ENST00000344297.8:c.2860A>G | ENSP00000342559.5:p.Ile954Val | |
| ENST00000400366.5:c.3148A>G | ENSP00000383217.3:p.Ile1050Val | |
| ENST00000400370.8:c.2191A>G | ENSP00000383221.3:p.Ile731Val | |
| ENST00000418097.7:c.3286A>G | ENSP00000393343.2:p.Ile1096Val | |
| ENST00000448424.6:c.3247A>G | ENSP00000416738.2:p.Ile1083Val | |
| ENST00000634296.1:c.1259A>G | ||
| ENST00000634308.1:c.*582A>G | ENSP00000489234.1:n.*582A>G | |
| ENST00000634620.1:n.4225A>G | ||
| ENST00000634810.1:n.2826A>G | ||
| ENST00000634844.1:c.3337A>G | ENSP00000489398.1:p.Ile1113Val | |
| NM_000053.3:c.3481A>G | NP_000044.2:p.Ile1161Val | |
| NM_001005918.2:c.2860A>G | NP_001005918.1:p.Ile954Val | |
| NM_001243182.1:c.3148A>G | NP_001230111.1:p.Ile1050Val | |
| XM_005266423.2:c.3385A>G | XP_005266480.1:p.Ile1129Val | |
| XM_005266424.3:c.3385A>G | XP_005266481.1:p.Ile1129Val | |
| XM_005266427.2:c.3247A>G | XP_005266484.1:p.Ile1083Val | |
| XM_005266428.1:c.3229A>G | XP_005266485.1:p.Ile1077Val | |
| XM_005266430.3:c.3481A>G | XP_005266487.1:p.Ile1161Val | |
| XM_005266431.2:c.3445A>G | XP_005266488.1:p.Ile1149Val | |
| XM_005266432.2:c.2995A>G | XP_005266489.1:p.Ile999Val | |
| XM_006719837.2:c.3385A>G | XP_006719900.1:p.Ile1129Val | |
| XM_006719838.1:c.1297A>G | XP_006719901.1:p.Ile433Val | |
| XM_006719839.1:c.1114A>G | XP_006719902.1:p.Ile372Val | |
| XM_011535117.1:c.3385A>G | XP_011533419.1:p.Ile1129Val | |
| XM_011535118.1:c.3346A>G | XP_011533420.1:p.Ile1116Val | |
| XM_011535119.1:c.3298A>G | XP_011533421.1:p.Ile1100Val | |
| XM_011535120.1:c.3067A>G | XP_011533422.1:p.Ile1023Val | |
| XM_011535121.1:c.2968A>G | XP_011533423.1:p.Ile990Val | |
| XM_011535122.1:c.2149A>G | XP_011533424.1:p.Ile717Val | |
| XR_941601.1:n.3700A>G | ||
| XR_941602.1:n.3700A>G | ||
| XR_941603.1:n.3700A>G | ||
| XR_941604.1:n.3700A>G | ||
| NM_001330578.1:c.3247A>G | NP_001317507.1:p.Ile1083Val | |
| NM_001330579.1:c.3229A>G | NP_001317508.1:p.Ile1077Val | |
| XM_005266424.4:c.3385A>G | XP_005266481.1:p.Ile1129Val | |
| XM_005266430.4:c.3481A>G | XP_005266487.1:p.Ile1161Val | |
| XM_005266431.4:c.3445A>G | XP_005266488.1:p.Ile1149Val | |
| XM_006719837.3:c.3385A>G | XP_006719900.1:p.Ile1129Val | |
| XM_011535117.3:c.3385A>G | XP_011533419.1:p.Ile1129Val | |
| XM_017020627.1:c.3385A>G | XP_016876116.1:p.Ile1129Val | |
| NM_000053.4:c.3481A>G MANE Select | NP_000044.2:p.Ile1161Val | |
| NM_001005918.3:c.2860A>G | NP_001005918.1:p.Ile954Val | |
| NM_001330579.2:c.3229A>G | NP_001317508.1:p.Ile1077Val | |
| NM_001243182.2:c.3148A>G | NP_001230111.1:p.Ile1050Val | |
| NM_001330578.2:c.3247A>G | NP_001317507.1:p.Ile1083Val |