Linked Data
ClinVar Variation Id:
1382435
ClinVar RCV Id:
RCV001890283
dbSNP Id:
rs780834522
ExAC:
1:154437621 C / T
gnomAD v2:
1-154437621-C-T
gnomAD v3:
1-154465145-C-T
gnomAD v4:
1-154465145-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154465145C>T , CM000663.2:g.154465145C>T | GRCh38 |
| NC_000001.10:g.154437621C>T , CM000663.1:g.154437621C>T | GRCh37 |
| NC_000001.9:g.152704245C>T | NCBI36 |
| NG_012087.1:g.64953C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368485.8:c.1172C>T MANE Select | ENSP00000357470.3:p.Thr391Met | |
| ENST00000344086.8:c.1078C>T | ENSP00000340589.4:p.Arg360Cys | |
| ENST00000368485.7:c.1172C>T | ENSP00000357470.3:p.Thr391Met | |
| ENST00000502679.1:n.485C>T | ||
| ENST00000507256.1:n.370C>T | ||
| NM_000565.3:c.1172C>T | NP_000556.1:p.Thr391Met | |
| NM_181359.2:c.1078C>T | NP_852004.1:p.Arg360Cys | |
| XM_005245139.1:c.936C>T | XP_005245196.1:p.Asp312= | |
| XM_005245140.1:c.*13C>T | XP_005245197.1:n.*13C>T | |
| XM_006711298.1:c.1220C>T | XP_006711361.1:p.Thr407Met | |
| XM_006711299.2:c.1126C>T | XP_006711362.1:p.Arg376Cys | |
| XM_005245139.2:c.936C>T | XP_005245196.1:p.Asp312= | |
| XM_005245140.3:c.*13C>T | XP_005245197.1:n.*13C>T | |
| XM_006711298.2:c.1220C>T | XP_006711361.1:p.Thr407Met | |
| XM_006711299.4:c.1126C>T | XP_006711362.1:p.Arg376Cys | |
| XM_017001199.2:c.1319C>T | XP_016856688.1:p.Thr440Met | |
| XM_017001200.2:c.1271C>T | XP_016856689.1:p.Thr424Met | |
| XM_017001201.2:c.*13C>T | XP_016856690.1:n.*13C>T | |
| NM_000565.4:c.1172C>T MANE Select | NP_000556.1:p.Thr391Met | |
| NM_181359.3:c.1078C>T | NP_852004.1:p.Arg360Cys | |
| NM_001382769.1:c.1271C>T | NP_001369698.1:p.Thr424Met | |
| NM_001382770.1:c.1265C>T | NP_001369699.1:p.Thr422Met | |
| NM_001382771.1:c.1220C>T | NP_001369700.1:p.Thr407Met | |
| NM_001382772.1:c.1166C>T | NP_001369701.1:p.Thr389Met | |
| NM_001382773.1:c.1126C>T | NP_001369702.1:p.Arg376Cys | |
| NM_001382774.1:c.812C>T | NP_001369703.1:p.Thr271Met |