Canonical Allele Identifier: CA457915434
Gene: AKR1D1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.137776615A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138091869A>C , CM000669.2:g.138091869A>C GRCh38
NC_000007.13:g.137776615A>C , CM000669.1:g.137776615A>C GRCh37
NC_000007.12:g.137427155A>C NCBI36
NG_023342.1:g.20438A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000242375.8:c.363A>C MANE Select ENSP00000242375.3:p.Val121=
ENST00000242375.7:c.363A>C ENSP00000242375.3:p.Val121=
ENST00000411726.6:c.363A>C ENSP00000402374.2:p.Val121=
ENST00000432161.5:c.363A>C ENSP00000389197.1:p.Val121=
ENST00000438242.1:c.195A>C ENSP00000397042.1:p.Val65=
ENST00000468877.2:n.273A>C
ENST00000470851.1:n.27A>C
NM_001190906.1:c.363A>C NP_001177835.1:p.Val121=
NM_001190907.1:c.363A>C NP_001177836.1:p.Val121=
NM_005989.3:c.363A>C NP_005980.1:p.Val121=
NM_005989.4:c.363A>C MANE Select NP_005980.1:p.Val121=
NM_001190906.2:c.363A>C NP_001177835.1:p.Val121=
NM_001190907.2:c.363A>C NP_001177836.1:p.Val121=