Canonical Allele Identifier: CA1746468649
Gene: AKR1D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138091873A= , CM000669.2:g.138091873A= GRCh38
NC_000007.13:g.137776619A= , CM000669.1:g.137776619A= GRCh37
NC_000007.12:g.137427159A= NCBI36
NG_023342.1:g.20442A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242375.8:c.367A= MANE Select ENSP00000242375.3:p.Met123=
ENST00000242375.7:c.367A= ENSP00000242375.3:p.Met123=
ENST00000411726.6:c.367A= ENSP00000402374.2:p.Met123=
ENST00000432161.5:c.367A= ENSP00000389197.1:p.Met123=
ENST00000438242.1:c.199A= ENSP00000397042.1:p.Met67=
ENST00000468877.2:n.277A=
ENST00000470851.1:n.31A=
NM_001190906.1:c.367A= NP_001177835.1:p.Met123=
NM_001190907.1:c.367A= NP_001177836.1:p.Met123=
NM_005989.3:c.367A= NP_005980.1:p.Met123=
NM_005989.4:c.367A= MANE Select NP_005980.1:p.Met123=
NM_001190906.2:c.367A= NP_001177835.1:p.Met123=
NM_001190907.2:c.367A= NP_001177836.1:p.Met123=