Canonical Allele Identifier: CA369359398

Gene: AKR1D1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242375.8:c.364C>G MANE Select	ENSP00000242375.3:p.Pro122Ala
ENST00000242375.7:c.364C>G	ENSP00000242375.3:p.Pro122Ala
ENST00000411726.6:c.364C>G	ENSP00000402374.2:p.Pro122Ala
ENST00000432161.5:c.364C>G	ENSP00000389197.1:p.Pro122Ala
ENST00000438242.1:c.196C>G	ENSP00000397042.1:p.Pro66Ala
ENST00000468877.2:n.274C>G
ENST00000470851.1:n.28C>G
NM_001190906.1:c.364C>G	NP_001177835.1:p.Pro122Ala
NM_001190907.1:c.364C>G	NP_001177836.1:p.Pro122Ala
NM_005989.3:c.364C>G	NP_005980.1:p.Pro122Ala
NM_005989.4:c.364C>G MANE Select	NP_005980.1:p.Pro122Ala
NM_001190906.2:c.364C>G	NP_001177835.1:p.Pro122Ala
NM_001190907.2:c.364C>G	NP_001177836.1:p.Pro122Ala