Canonical Allele Identifier: CA1746468635
Gene: AKR1D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138091835A= , CM000669.2:g.138091835A= GRCh38
NC_000007.13:g.137776581A= , CM000669.1:g.137776581A= GRCh37
NC_000007.12:g.137427121A= NCBI36
NG_023342.1:g.20404A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242375.8:c.329A= MANE Select ENSP00000242375.3:p.Gln110=
ENST00000242375.7:c.329A= ENSP00000242375.3:p.Gln110=
ENST00000411726.6:c.329A= ENSP00000402374.2:p.Gln110=
ENST00000432161.5:c.329A= ENSP00000389197.1:p.Gln110=
ENST00000438242.1:c.161A= ENSP00000397042.1:p.Gln54=
ENST00000468877.2:n.239A=
NM_001190906.1:c.329A= NP_001177835.1:p.Gln110=
NM_001190907.1:c.329A= NP_001177836.1:p.Gln110=
NM_005989.3:c.329A= NP_005980.1:p.Gln110=
NM_005989.4:c.329A= MANE Select NP_005980.1:p.Gln110=
NM_001190906.2:c.329A= NP_001177835.1:p.Gln110=
NM_001190907.2:c.329A= NP_001177836.1:p.Gln110=