Linked Data
ClinVar Variation Id:
644235
ClinVar RCV Id:
RCV000798114
dbSNP Id:
rs140710297
ExAC:
15:44876153 C / T
gnomAD v2:
15-44876153-C-T
gnomAD v3:
15-44583955-C-T
gnomAD v4:
15-44583955-C-T
COSMIC:
COSM379056
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.44583955C>T , CM000677.2:g.44583955C>T | GRCh38 |
| NC_000015.9:g.44876153C>T , CM000677.1:g.44876153C>T | GRCh37 |
| NC_000015.8:g.42663445C>T | NCBI36 |
| NG_008885.1:g.84724G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559511.6:c.5725G>A | ENSP00000453246.2:p.Ala1909Thr | |
| ENST00000561391.2:n.1953G>A | ||
| ENST00000682065.1:c.5581G>A | ENSP00000507025.1:p.Ala1861Thr | |
| ENST00000682460.1:c.*1982G>A | ENSP00000508334.1:n.*1982G>A | |
| ENST00000682495.1:c.*2217G>A | ENSP00000507166.1:n.*2217G>A | |
| ENST00000682669.1:c.5524G>A | ENSP00000507782.1:p.Ala1842Thr | |
| ENST00000683186.1:c.*2488G>A | ENSP00000507268.1:n.*2488G>A | |
| ENST00000683496.1:c.5725G>A | ENSP00000506968.1:p.Ala1909Thr | |
| ENST00000683734.1:c.5725G>A | ENSP00000508319.1:p.Ala1909Thr | |
| ENST00000683753.1:n.4771G>A | ||
| ENST00000684038.1:c.*2145G>A | ENSP00000507141.1:n.*2145G>A | |
| ENST00000684235.1:c.5725G>A | ENSP00000508295.1:p.Ala1909Thr | |
| ENST00000684676.1:c.5516-20G>A | ENSP00000506948.1:n.5516-20G>A | |
| ENST00000261866.12:c.5725G>A MANE Select | ENSP00000261866.7:p.Ala1909Thr | |
| ENST00000261866.11:c.5725G>A | ENSP00000261866.7:p.Ala1909Thr | |
| ENST00000427534.6:c.5725G>A | ENSP00000396110.2:p.Ala1909Thr | |
| ENST00000535302.6:c.5725G>A | ENSP00000445278.2:p.Ala1909Thr | |
| ENST00000558319.5:c.5725G>A | ENSP00000453599.1:p.Ala1909Thr | |
| ENST00000559511.5:c.573G>A | ||
| ENST00000559822.1:c.288-20G>A | ||
| NM_001160227.1:c.5725G>A | NP_001153699.1:p.Ala1909Thr | |
| NM_025137.3:c.5725G>A | NP_079413.3:p.Ala1909Thr | |
| XM_005254695.3:c.5467G>A | XP_005254752.1:p.Ala1823Thr | |
| XM_006720700.1:c.5581G>A | XP_006720763.1:p.Ala1861Thr | |
| XM_017022634.1:c.5725G>A | XP_016878123.1:p.Ala1909Thr | |
| XM_017022636.1:c.2602G>A | XP_016878125.1:p.Ala868Thr | |
| NM_025137.4:c.5725G>A MANE Select | NP_079413.3:p.Ala1909Thr | |
| NM_001160227.2:c.5725G>A | NP_001153699.1:p.Ala1909Thr |