Canonical Allele Identifier: CA369359371

Gene: AKR1D1

Linked Data

• MyVariant Identifiers: chr7:g.137776604A>T (hg19) ; chr7:g.138091858A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.138091858A>T , CM000669.2:g.138091858A>T	GRCh38
NC_000007.13:g.137776604A>T , CM000669.1:g.137776604A>T	GRCh37
NC_000007.12:g.137427144A>T	NCBI36
NG_023342.1:g.20427A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242375.8:c.352A>T MANE Select	ENSP00000242375.3:p.Ile118Phe
ENST00000242375.7:c.352A>T	ENSP00000242375.3:p.Ile118Phe
ENST00000411726.6:c.352A>T	ENSP00000402374.2:p.Ile118Phe
ENST00000432161.5:c.352A>T	ENSP00000389197.1:p.Ile118Phe
ENST00000438242.1:c.184A>T	ENSP00000397042.1:p.Ile62Phe
ENST00000468877.2:n.262A>T
ENST00000470851.1:n.16A>T
NM_001190906.1:c.352A>T	NP_001177835.1:p.Ile118Phe
NM_001190907.1:c.352A>T	NP_001177836.1:p.Ile118Phe
NM_005989.3:c.352A>T	NP_005980.1:p.Ile118Phe
NM_005989.4:c.352A>T MANE Select	NP_005980.1:p.Ile118Phe
NM_001190906.2:c.352A>T	NP_001177835.1:p.Ile118Phe
NM_001190907.2:c.352A>T	NP_001177836.1:p.Ile118Phe