Canonical Allele Identifier: CA457915312
Gene: AKR1D1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.137776537A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138091791A>T , CM000669.2:g.138091791A>T GRCh38
NC_000007.13:g.137776537A>T , CM000669.1:g.137776537A>T GRCh37
NC_000007.12:g.137427077A>T NCBI36
NG_023342.1:g.20360A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000242375.8:c.285A>T MANE Select ENSP00000242375.3:p.Pro95=
ENST00000242375.7:c.285A>T ENSP00000242375.3:p.Pro95=
ENST00000411726.6:c.285A>T ENSP00000402374.2:p.Pro95=
ENST00000432161.5:c.285A>T ENSP00000389197.1:p.Pro95=
ENST00000438242.1:c.117A>T ENSP00000397042.1:p.Pro39=
ENST00000468877.2:n.222-27A>T
NM_001190906.1:c.285A>T NP_001177835.1:p.Pro95=
NM_001190907.1:c.285A>T NP_001177836.1:p.Pro95=
NM_005989.3:c.285A>T NP_005980.1:p.Pro95=
NM_005989.4:c.285A>T MANE Select NP_005980.1:p.Pro95=
NM_001190906.2:c.285A>T NP_001177835.1:p.Pro95=
NM_001190907.2:c.285A>T NP_001177836.1:p.Pro95=