Canonical Allele Identifier: CA1746468644
Gene: AKR1D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138091855T= , CM000669.2:g.138091855T= GRCh38
NC_000007.13:g.137776601T= , CM000669.1:g.137776601T= GRCh37
NC_000007.12:g.137427141T= NCBI36
NG_023342.1:g.20424T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242375.8:c.349T= MANE Select ENSP00000242375.3:p.Tyr117=
ENST00000242375.7:c.349T= ENSP00000242375.3:p.Tyr117=
ENST00000411726.6:c.349T= ENSP00000402374.2:p.Tyr117=
ENST00000432161.5:c.349T= ENSP00000389197.1:p.Tyr117=
ENST00000438242.1:c.181T= ENSP00000397042.1:p.Tyr61=
ENST00000468877.2:n.259T=
ENST00000470851.1:n.13T=
NM_001190906.1:c.349T= NP_001177835.1:p.Tyr117=
NM_001190907.1:c.349T= NP_001177836.1:p.Tyr117=
NM_005989.3:c.349T= NP_005980.1:p.Tyr117=
NM_005989.4:c.349T= MANE Select NP_005980.1:p.Tyr117=
NM_001190906.2:c.349T= NP_001177835.1:p.Tyr117=
NM_001190907.2:c.349T= NP_001177836.1:p.Tyr117=