Canonical Allele Identifier: CA369359184

Gene: AKR1D1

Linked Data

• MyVariant Identifiers: chr7:g.137776526A>G (hg19) ; chr7:g.138091780A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.138091780A>G , CM000669.2:g.138091780A>G	GRCh38
NC_000007.13:g.137776526A>G , CM000669.1:g.137776526A>G	GRCh37
NC_000007.12:g.137427066A>G	NCBI36
NG_023342.1:g.20349A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242375.8:c.274A>G MANE Select	ENSP00000242375.3:p.Asn92Asp
ENST00000242375.7:c.274A>G	ENSP00000242375.3:p.Asn92Asp
ENST00000411726.6:c.274A>G	ENSP00000402374.2:p.Asn92Asp
ENST00000432161.5:c.274A>G	ENSP00000389197.1:p.Asn92Asp
ENST00000438242.1:c.106A>G	ENSP00000397042.1:p.Asn36Asp
ENST00000468877.2:n.222-38A>G
NM_001190906.1:c.274A>G	NP_001177835.1:p.Asn92Asp
NM_001190907.1:c.274A>G	NP_001177836.1:p.Asn92Asp
NM_005989.3:c.274A>G	NP_005980.1:p.Asn92Asp
NM_005989.4:c.274A>G MANE Select	NP_005980.1:p.Asn92Asp
NM_001190906.2:c.274A>G	NP_001177835.1:p.Asn92Asp
NM_001190907.2:c.274A>G	NP_001177836.1:p.Asn92Asp