Canonical Allele Identifier: CA369359317

Gene: AKR1D1

Linked Data

• MyVariant Identifiers: chr7:g.137776580C>A (hg19) ; chr7:g.138091834C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.138091834C>A , CM000669.2:g.138091834C>A	GRCh38
NC_000007.13:g.137776580C>A , CM000669.1:g.137776580C>A	GRCh37
NC_000007.12:g.137427120C>A	NCBI36
NG_023342.1:g.20403C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000242375.8:c.328C>A MANE Select	ENSP00000242375.3:p.Gln110Lys
ENST00000242375.7:c.328C>A	ENSP00000242375.3:p.Gln110Lys
ENST00000411726.6:c.328C>A	ENSP00000402374.2:p.Gln110Lys
ENST00000432161.5:c.328C>A	ENSP00000389197.1:p.Gln110Lys
ENST00000438242.1:c.160C>A	ENSP00000397042.1:p.Gln54Lys
ENST00000468877.2:n.238C>A
NM_001190906.1:c.328C>A	NP_001177835.1:p.Gln110Lys
NM_001190907.1:c.328C>A	NP_001177836.1:p.Gln110Lys
NM_005989.3:c.328C>A	NP_005980.1:p.Gln110Lys
NM_005989.4:c.328C>A MANE Select	NP_005980.1:p.Gln110Lys
NM_001190906.2:c.328C>A	NP_001177835.1:p.Gln110Lys
NM_001190907.2:c.328C>A	NP_001177836.1:p.Gln110Lys