Linked Data
ClinVar Variation Id:
1018417
ClinVar RCV Id:
RCV001317714
dbSNP Id:
rs947155109
gnomAD v4:
16-23641138-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23641138T>A , CM000678.2:g.23641138T>A | GRCh38 |
| NC_000016.9:g.23652459T>A , CM000678.1:g.23652459T>A | GRCh37 |
| NC_000016.8:g.23559960T>A | NCBI36 |
| NG_007406.1:g.5220A>T , LRG_308:g.5220A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000561514.3:c.-833A>T | ENSP00000460666.3:n.-833A>T | |
| ENST00000565038.2:c.20A>T | ENSP00000459882.2:p.Lys7Met | |
| ENST00000566069.6:c.20A>T | ENSP00000459237.2:p.Lys7Met | |
| ENST00000697377.2:c.-220A>T | ENSP00000513286.2:n.-220A>T | |
| ENST00000697379.2:c.-126A>T | ENSP00000513287.2:n.-126A>T | |
| ENST00000561514.2:c.-1724A>T | ENSP00000460666.2:n.-1724A>T | |
| ENST00000697374.1:c.-1315A>T | ENSP00000513284.1:n.-1315A>T | |
| ENST00000697376.1:c.-1036A>T | ENSP00000513285.1:n.-1036A>T | |
| ENST00000697377.1:c.-1111A>T | ENSP00000513286.1:n.-1111A>T | |
| ENST00000697379.1:c.-1017A>T | ENSP00000513287.1:n.-1017A>T | |
| ENST00000697382.1:c.-1775A>T | ENSP00000513288.1:n.-1775A>T | |
| ENST00000697383.1:c.20A>T | ENSP00000513289.1:p.Lys7Met | |
| ENST00000697384.1:n.174A>T | ||
| ENST00000261584.9:c.20A>T MANE Select | ENSP00000261584.4:p.Lys7Met | |
| ENST00000261584.8:c.20A>T | ENSP00000261584.4:p.Lys7Met | |
| ENST00000567003.1:n.164A>T | ||
| ENST00000568219.5:c.-849A>T | ENSP00000454703.2:n.-849A>T | |
| NM_024675.3:c.20A>T , LRG_308t1:c.20A>T | NP_078951.2:p.Lys7Met | |
| XM_011545948.1:c.-1000A>T | XP_011544250.1:n.-1000A>T | |
| XM_011545946.2:c.-833A>T | XP_011544248.1:n.-833A>T | |
| XM_011545947.2:c.-833A>T | XP_011544249.1:n.-833A>T | |
| XM_011545948.2:c.-1000A>T | XP_011544250.1:n.-1000A>T | |
| XM_017023671.1:c.-833A>T | XP_016879160.1:n.-833A>T | |
| XM_017023672.2:c.20A>T | XP_016879161.1:p.Lys7Met | |
| XM_017023673.2:c.20A>T | XP_016879162.1:p.Lys7Met | |
| NM_024675.4:c.20A>T MANE Select | NP_078951.2:p.Lys7Met |