Canonical Allele Identifier: CA1746475168
Gene: AKR1D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138107506C= , CM000669.2:g.138107506C= GRCh38
NC_000007.13:g.137792252C= , CM000669.1:g.137792252C= GRCh37
NC_000007.12:g.137442792C= NCBI36
NG_023342.1:g.36075C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242375.8:c.781C= MANE Select ENSP00000242375.3:p.Arg261=
ENST00000242375.7:c.781C= ENSP00000242375.3:p.Arg261=
ENST00000411726.6:c.658C= ENSP00000402374.2:p.Arg220=
ENST00000432161.5:c.781C= ENSP00000389197.1:p.Arg261=
ENST00000468877.2:n.804C=
NM_001190906.1:c.658C= NP_001177835.1:p.Arg220=
NM_001190907.1:c.781C= NP_001177836.1:p.Arg261=
NM_005989.3:c.781C= NP_005980.1:p.Arg261=
NM_005989.4:c.781C= MANE Select NP_005980.1:p.Arg261=
NM_001190906.2:c.658C= NP_001177835.1:p.Arg220=
NM_001190907.2:c.781C= NP_001177836.1:p.Arg261=