Canonical Allele Identifier: CA1746468624

Gene: AKR1D1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.138091808C= , CM000669.2:g.138091808C=	GRCh38
NC_000007.13:g.137776554C= , CM000669.1:g.137776554C=	GRCh37
NC_000007.12:g.137427094C=	NCBI36
NG_023342.1:g.20377C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242375.8:c.302C= MANE Select	ENSP00000242375.3:p.Thr101=
ENST00000242375.7:c.302C=	ENSP00000242375.3:p.Thr101=
ENST00000411726.6:c.302C=	ENSP00000402374.2:p.Thr101=
ENST00000432161.5:c.302C=	ENSP00000389197.1:p.Thr101=
ENST00000438242.1:c.134C=	ENSP00000397042.1:p.Thr45=
ENST00000468877.2:n.222-10C=
NM_001190906.1:c.302C=	NP_001177835.1:p.Thr101=
NM_001190907.1:c.302C=	NP_001177836.1:p.Thr101=
NM_005989.3:c.302C=	NP_005980.1:p.Thr101=
NM_005989.4:c.302C= MANE Select	NP_005980.1:p.Thr101=
NM_001190906.2:c.302C=	NP_001177835.1:p.Thr101=
NM_001190907.2:c.302C=	NP_001177836.1:p.Thr101=