Canonical Allele Identifier: CA369359397

Gene: AKR1D1

Linked Data

• MyVariant Identifiers: chr7:g.137776616C>A (hg19) ; chr7:g.138091870C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.138091870C>A , CM000669.2:g.138091870C>A	GRCh38
NC_000007.13:g.137776616C>A , CM000669.1:g.137776616C>A	GRCh37
NC_000007.12:g.137427156C>A	NCBI36
NG_023342.1:g.20439C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242375.8:c.364C>A MANE Select	ENSP00000242375.3:p.Pro122Thr
ENST00000242375.7:c.364C>A	ENSP00000242375.3:p.Pro122Thr
ENST00000411726.6:c.364C>A	ENSP00000402374.2:p.Pro122Thr
ENST00000432161.5:c.364C>A	ENSP00000389197.1:p.Pro122Thr
ENST00000438242.1:c.196C>A	ENSP00000397042.1:p.Pro66Thr
ENST00000468877.2:n.274C>A
ENST00000470851.1:n.28C>A
NM_001190906.1:c.364C>A	NP_001177835.1:p.Pro122Thr
NM_001190907.1:c.364C>A	NP_001177836.1:p.Pro122Thr
NM_005989.3:c.364C>A	NP_005980.1:p.Pro122Thr
NM_005989.4:c.364C>A MANE Select	NP_005980.1:p.Pro122Thr
NM_001190906.2:c.364C>A	NP_001177835.1:p.Pro122Thr
NM_001190907.2:c.364C>A	NP_001177836.1:p.Pro122Thr