Linked Data
ClinVar Variation Id:
1744986
ClinVar RCV Id:
RCV002335699
dbSNP Id:
rs2154471430
gnomAD v4:
17-43094340-G-A
MyVariant Identifiers:
chr17:g.41246357G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43094340G>A , CM000679.2:g.43094340G>A | GRCh38 |
| NC_000017.10:g.41246357G>A , CM000679.1:g.41246357G>A | GRCh37 |
| NC_000017.9:g.38499883G>A | NCBI36 |
| NG_005905.2:g.123644C>T , LRG_292:g.123644C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000354071.8:n.1255C>T | ||
| ENST00000461574.2:c.1191C>T | ENSP00000417241.2:p.Asp397= | |
| ENST00000470026.6:c.1191C>T | ENSP00000419274.2:p.Asp397= | |
| ENST00000473961.6:c.1065C>T | ENSP00000420201.2:p.Asp355= | |
| ENST00000476777.6:c.1188C>T | ENSP00000417554.2:p.Asp396= | |
| ENST00000477152.6:c.1113C>T | ENSP00000419988.2:p.Asp371= | |
| ENST00000478531.6:c.784+404C>T | ENSP00000420412.2:n.784+404C>T | |
| ENST00000489037.2:c.1113C>T | ENSP00000420781.2:p.Asp371= | |
| ENST00000493919.6:c.646+404C>T | ENSP00000418819.2:n.646+404C>T | |
| ENST00000494123.6:c.1191C>T | ENSP00000419103.2:p.Asp397= | |
| ENST00000497488.2:c.303C>T | ENSP00000418986.2:p.Asp101= | |
| ENST00000618469.2:c.1191C>T | ENSP00000478114.2:p.Asp397= | |
| ENST00000634433.2:c.1068C>T | ENSP00000489431.2:p.Asp356= | |
| ENST00000644379.2:c.1191C>T | ENSP00000496570.2:p.Asp397= | |
| ENST00000644555.2:c.646+404C>T | ENSP00000494614.2:n.646+404C>T | |
| ENST00000652672.2:c.1050C>T | ENSP00000498906.2:p.Asp350= | |
| ENST00000484087.6:c.664+404C>T | ENSP00000419481.2:n.664+404C>T | |
| ENST00000700182.1:c.706+404C>T | ENSP00000514849.1:n.706+404C>T | |
| ENST00000700183.1:c.*1199C>T | ENSP00000514850.1:n.*1199C>T | |
| ENST00000357654.9:c.1191C>T MANE Select | ENSP00000350283.3:p.Asp397= | |
| ENST00000471181.7:c.1191C>T | ENSP00000418960.2:p.Asp397= | |
| ENST00000652672.1:c.1050C>T | ENSP00000498906.1:p.Asp350= | |
| ENST00000352993.7:c.670+1506C>T | ENSP00000312236.5:n.670+1506C>T | |
| ENST00000354071.7:c.1191C>T | ENSP00000326002.7:p.Asp397= | |
| ENST00000357654.7:c.1191C>T | ENSP00000350283.3:p.Asp397= | |
| ENST00000412061.3:c.542C>T | ||
| ENST00000461221.5:c.*974C>T | ENSP00000418548.1:n.*974C>T | |
| ENST00000468300.5:c.787+404C>T | ENSP00000417148.1:n.787+404C>T | |
| ENST00000470026.5:c.1191C>T | ENSP00000419274.1:p.Asp397= | |
| ENST00000471181.6:c.1191C>T | ENSP00000418960.2:p.Asp397= | |
| ENST00000473961.5:c.788C>T | ||
| ENST00000477152.5:c.1113C>T | ENSP00000419988.1:p.Asp371= | |
| ENST00000478531.5:c.784+404C>T | ENSP00000420412.1:n.784+404C>T | |
| ENST00000484087.5:c.409+404C>T | ENSP00000419481.1:n.409+404C>T | |
| ENST00000487825.5:c.412+404C>T | ENSP00000418212.1:n.412+404C>T | |
| ENST00000491747.6:c.787+404C>T | ENSP00000420705.2:n.787+404C>T | |
| ENST00000492859.5:c.*1127C>T | ENSP00000420253.1:n.*1127C>T | |
| ENST00000493795.5:c.1050C>T | ENSP00000418775.1:p.Asp350= | |
| ENST00000493919.5:c.646+404C>T | ENSP00000418819.1:n.646+404C>T | |
| ENST00000494123.5:c.1191C>T | ENSP00000419103.1:p.Asp397= | |
| ENST00000497488.1:c.303C>T | ENSP00000418986.1:p.Asp101= | |
| ENST00000586385.5:c.5-30389C>T | ENSP00000465818.1:n.5-30389C>T | |
| ENST00000591534.5:c.-43-19819C>T | ENSP00000467329.1:n.-43-19819C>T | |
| ENST00000591849.5:c.-99+30931C>T | ENSP00000465347.1:n.-99+30931C>T | |
| ENST00000634433.1:c.1068C>T | ENSP00000489431.1:p.Asp356= | |
| NM_007294.3:c.1191C>T , LRG_292t1:c.1191C>T | NP_009225.1:p.Asp397= | |
| NM_007297.3:c.1050C>T | NP_009228.2:p.Asp350= | |
| NM_007298.3:c.787+404C>T | NP_009229.2:n.787+404C>T | |
| NM_007299.3:c.787+404C>T | NP_009230.2:n.787+404C>T | |
| NM_007300.3:c.1191C>T | NP_009231.2:p.Asp397= | |
| NR_027676.1:n.1327C>T | ||
| NM_007294.4:c.1191C>T MANE Select | NP_009225.1:p.Asp397= | |
| NM_007297.4:c.1050C>T | NP_009228.2:p.Asp350= | |
| NM_007299.4:c.787+404C>T | NP_009230.2:n.787+404C>T | |
| NM_007300.4:c.1191C>T | NP_009231.2:p.Asp397= | |
| NR_027676.2:n.1368C>T |