Canonical Allele Identifier: CA457915362
Gene: AKR1D1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.137776579C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138091833C>G , CM000669.2:g.138091833C>G GRCh38
NC_000007.13:g.137776579C>G , CM000669.1:g.137776579C>G GRCh37
NC_000007.12:g.137427119C>G NCBI36
NG_023342.1:g.20402C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000242375.8:c.327C>G MANE Select ENSP00000242375.3:p.Leu109=
ENST00000242375.7:c.327C>G ENSP00000242375.3:p.Leu109=
ENST00000411726.6:c.327C>G ENSP00000402374.2:p.Leu109=
ENST00000432161.5:c.327C>G ENSP00000389197.1:p.Leu109=
ENST00000438242.1:c.159C>G ENSP00000397042.1:p.Leu53=
ENST00000468877.2:n.237C>G
NM_001190906.1:c.327C>G NP_001177835.1:p.Leu109=
NM_001190907.1:c.327C>G NP_001177836.1:p.Leu109=
NM_005989.3:c.327C>G NP_005980.1:p.Leu109=
NM_005989.4:c.327C>G MANE Select NP_005980.1:p.Leu109=
NM_001190906.2:c.327C>G NP_001177835.1:p.Leu109=
NM_001190907.2:c.327C>G NP_001177836.1:p.Leu109=