Linked Data
ClinVar Variation Id:
653845
ClinVar RCV Id:
RCV000809683
dbSNP Id:
rs80357473
gnomAD v2:
17-41234579-A-T
gnomAD v3:
17-43082562-A-T
gnomAD v4:
17-43082562-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43082562A>T , CM000679.2:g.43082562A>T | GRCh38 |
| NC_000017.10:g.41234579A>T , CM000679.1:g.41234579A>T | GRCh37 |
| NC_000017.9:g.38488105A>T | NCBI36 |
| NG_005905.2:g.135422T>A , LRG_292:g.135422T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461574.2:c.4199T>A | ENSP00000417241.2:p.Met1400Lys | |
| ENST00000470026.6:c.4199T>A | ENSP00000419274.2:p.Met1400Lys | |
| ENST00000473961.6:c.4073T>A | ENSP00000420201.2:p.Met1358Lys | |
| ENST00000476777.6:c.4193T>A | ENSP00000417554.2:p.Met1398Lys | |
| ENST00000477152.6:c.4121T>A | ENSP00000419988.2:p.Met1374Lys | |
| ENST00000478531.6:c.887T>A | ENSP00000420412.2:p.Met296Lys | |
| ENST00000489037.2:c.4121T>A | ENSP00000420781.2:p.Met1374Lys | |
| ENST00000493919.6:c.749T>A | ENSP00000418819.2:p.Met250Lys | |
| ENST00000494123.6:c.4199T>A | ENSP00000419103.2:p.Met1400Lys | |
| ENST00000497488.2:c.3311T>A | ENSP00000418986.2:p.Met1104Lys | |
| ENST00000618469.2:c.4199T>A | ENSP00000478114.2:p.Met1400Lys | |
| ENST00000634433.2:c.4076T>A | ENSP00000489431.2:p.Met1359Lys | |
| ENST00000644379.2:c.4199T>A | ENSP00000496570.2:p.Met1400Lys | |
| ENST00000644555.2:c.749T>A | ENSP00000494614.2:p.Met250Lys | |
| ENST00000652672.2:c.4058T>A | ENSP00000498906.2:p.Met1353Lys | |
| ENST00000484087.6:c.764T>A | ENSP00000419481.2:p.Met255Lys | |
| ENST00000700182.1:c.809T>A | ENSP00000514849.1:p.Met270Lys | |
| ENST00000357654.9:c.4199T>A MANE Select | ENSP00000350283.3:p.Met1400Lys | |
| ENST00000471181.7:c.4199T>A | ENSP00000418960.2:p.Met1400Lys | |
| ENST00000644379.1:c.520T>A | ||
| ENST00000352993.7:c.773T>A | ENSP00000312236.5:p.Met258Lys | |
| ENST00000357654.7:c.4199T>A | ENSP00000350283.3:p.Met1400Lys | |
| ENST00000461221.5:c.*3982T>A | ENSP00000418548.1:n.*3982T>A | |
| ENST00000461574.1:c.493T>A | ||
| ENST00000468300.5:c.890T>A | ENSP00000417148.1:p.Met297Lys | |
| ENST00000471181.6:c.4199T>A | ENSP00000418960.2:p.Met1400Lys | |
| ENST00000478531.5:c.887T>A | ENSP00000420412.1:p.Met296Lys | |
| ENST00000484087.5:c.512T>A | ENSP00000419481.1:p.Met171Lys | |
| ENST00000487825.5:c.515T>A | ENSP00000418212.1:p.Met172Lys | |
| ENST00000491747.6:c.890T>A | ENSP00000420705.2:p.Met297Lys | |
| ENST00000493795.5:c.4058T>A | ENSP00000418775.1:p.Met1353Lys | |
| ENST00000493919.5:c.749T>A | ENSP00000418819.1:p.Met250Lys | |
| ENST00000586385.5:c.5-18611T>A | ENSP00000465818.1:n.5-18611T>A | |
| ENST00000591534.5:c.-43-8041T>A | ENSP00000467329.1:n.-43-8041T>A | |
| ENST00000591849.5:c.-98-32372T>A | ENSP00000465347.1:n.-98-32372T>A | |
| ENST00000621897.1:n.93T>A | ||
| NM_007294.3:c.4199T>A , LRG_292t1:c.4199T>A | NP_009225.1:p.Met1400Lys | |
| NM_007297.3:c.4058T>A | NP_009228.2:p.Met1353Lys | |
| NM_007298.3:c.890T>A | NP_009229.2:p.Met297Lys | |
| NM_007299.3:c.890T>A | NP_009230.2:p.Met297Lys | |
| NM_007300.3:c.4199T>A | NP_009231.2:p.Met1400Lys | |
| NR_027676.1:n.4335T>A | ||
| NM_007294.4:c.4199T>A MANE Select | NP_009225.1:p.Met1400Lys | |
| NM_007297.4:c.4058T>A | NP_009228.2:p.Met1353Lys | |
| NM_007299.4:c.890T>A | NP_009230.2:p.Met297Lys | |
| NM_007300.4:c.4199T>A | NP_009231.2:p.Met1400Lys | |
| NR_027676.2:n.4376T>A |