Canonical Allele Identifier: CA4502640

Gene: AKR1D1

Linked Data

• dbSNP Id: rs182534921
• ExAC: 7:137776506 T / A
• gnomAD v2: 7-137776506-T-A
• gnomAD v3: 7-138091760-T-A
• gnomAD v4: 7-138091760-T-A
• MyVariant Identifiers: chr7:g.137776506T>A (hg19) ; chr7:g.138091760T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.138091760T>A , CM000669.2:g.138091760T>A	GRCh38
NC_000007.13:g.137776506T>A , CM000669.1:g.137776506T>A	GRCh37
NC_000007.12:g.137427046T>A	NCBI36
NG_023342.1:g.20329T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242375.8:c.262-8T>A MANE Select	ENSP00000242375.3:n.262-8T>A
ENST00000242375.7:c.262-8T>A	ENSP00000242375.3:n.262-8T>A
ENST00000411726.6:c.262-8T>A	ENSP00000402374.2:n.262-8T>A
ENST00000432161.5:c.262-8T>A	ENSP00000389197.1:n.262-8T>A
ENST00000438242.1:c.94-8T>A	ENSP00000397042.1:n.94-8T>A
ENST00000468877.2:n.222-58T>A
NM_001190906.1:c.262-8T>A	NP_001177835.1:n.262-8T>A
NM_001190907.1:c.262-8T>A	NP_001177836.1:n.262-8T>A
NM_005989.3:c.262-8T>A	NP_005980.1:n.262-8T>A
NM_005989.4:c.262-8T>A MANE Select	NP_005980.1:n.262-8T>A
NM_001190906.2:c.262-8T>A	NP_001177835.1:n.262-8T>A
NM_001190907.2:c.262-8T>A	NP_001177836.1:n.262-8T>A