Linked Data
ClinVar Variation Id:
241318
dbSNP Id:
rs61744648
ExAC:
14:45644474 T / G
gnomAD v2:
14-45644474-T-G
gnomAD v3:
14-45175271-T-G
gnomAD v4:
14-45175271-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.45175271T>G , CM000676.2:g.45175271T>G | GRCh38 |
| NC_000014.8:g.45644474T>G , CM000676.1:g.45644474T>G | GRCh37 |
| NC_000014.7:g.44714224T>G | NCBI36 |
| NG_007417.1:g.44339T>G , LRG_502:g.44339T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000554809.6:c.729T>G | ENSP00000450632.2:p.Ile243Met | |
| ENST00000556250.6:c.2310T>G | ENSP00000452033.2:p.Ile770Met | |
| ENST00000696641.1:c.2358T>G | ENSP00000512774.1:p.Ile786Met | |
| ENST00000696642.1:c.*1328T>G | ENSP00000512775.1:n.*1328T>G | |
| ENST00000696646.1:c.*1328T>G | ENSP00000512777.1:n.*1328T>G | |
| ENST00000696647.1:c.2517T>G | ENSP00000512778.1:p.Ile839Met | |
| ENST00000696648.1:c.*542T>G | ENSP00000512779.1:n.*542T>G | |
| ENST00000696649.1:c.2361T>G | ENSP00000512780.1:p.Ile787Met | |
| ENST00000696650.1:n.2465T>G | ||
| ENST00000696658.1:n.3067T>G | ||
| ENST00000696659.1:c.515T>G | ||
| ENST00000696663.1:c.1334T>G | ||
| ENST00000696664.1:c.1334T>G | ||
| ENST00000696675.1:c.2517T>G | ENSP00000512799.1:p.Ile839Met | |
| ENST00000696683.1:c.1334T>G | ||
| ENST00000696684.1:c.1334T>G | ||
| ENST00000696685.1:c.1334T>G | ||
| ENST00000267430.10:c.2517T>G MANE Select | ENSP00000267430.5:p.Ile839Met | |
| ENST00000267430.9:c.2517T>G | ENSP00000267430.5:p.Ile839Met | |
| ENST00000542564.6:c.2439T>G | ENSP00000442493.2:p.Ile813Met | |
| ENST00000556250.5:c.1065T>G | ENSP00000452033.1:p.Ile355Met | |
| NM_001308133.1:c.2439T>G | NP_001295062.1:p.Ile813Met | |
| NM_020937.2:c.2517T>G , LRG_502t1:c.2517T>G | NP_065988.1:p.Ile839Met | |
| NM_020937.3:c.2517T>G | NP_065988.1:p.Ile839Met | |
| XM_011537034.1:c.2517T>G | XP_011535336.1:p.Ile839Met | |
| XM_011537035.1:c.2439T>G | XP_011535337.1:p.Ile813Met | |
| XM_011537036.1:c.2517T>G | XP_011535338.1:p.Ile839Met | |
| XM_011537037.1:c.531T>G | XP_011535339.1:p.Ile177Met | |
| XM_011537034.2:c.2517T>G | XP_011535336.1:p.Ile839Met | |
| XM_011537035.3:c.2439T>G | XP_011535337.1:p.Ile813Met | |
| XM_011537037.3:c.531T>G | XP_011535339.1:p.Ile177Met | |
| XM_017021523.1:c.2517T>G | XP_016877012.1:p.Ile839Met | |
| XM_017021524.2:c.1554T>G | XP_016877013.1:p.Ile518Met | |
| XM_017021525.2:c.1332T>G | XP_016877014.1:p.Ile444Met | |
| XM_017021526.2:c.1332T>G | XP_016877015.1:p.Ile444Met | |
| XM_017021527.1:c.1332T>G | XP_016877016.1:p.Ile444Met | |
| XR_001750470.1:n.2609T>G | ||
| XR_001750471.2:n.2609T>G | ||
| XR_001750472.1:n.2609T>G | ||
| NM_020937.4:c.2517T>G MANE Select | NP_065988.1:p.Ile839Met | |
| NM_001308133.2:c.2439T>G | NP_001295062.1:p.Ile813Met |