Canonical Allele Identifier: CA369359267

Gene: AKR1D1

Linked Data

• dbSNP Id: rs1239574385
• gnomAD v2: 7-137776554-C-T
• gnomAD v4: 7-138091808-C-T
• MyVariant Identifiers: chr7:g.137776554C>T (hg19) ; chr7:g.138091808C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.138091808C>T , CM000669.2:g.138091808C>T	GRCh38
NC_000007.13:g.137776554C>T , CM000669.1:g.137776554C>T	GRCh37
NC_000007.12:g.137427094C>T	NCBI36
NG_023342.1:g.20377C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242375.8:c.302C>T MANE Select	ENSP00000242375.3:p.Thr101Ile
ENST00000242375.7:c.302C>T	ENSP00000242375.3:p.Thr101Ile
ENST00000411726.6:c.302C>T	ENSP00000402374.2:p.Thr101Ile
ENST00000432161.5:c.302C>T	ENSP00000389197.1:p.Thr101Ile
ENST00000438242.1:c.134C>T	ENSP00000397042.1:p.Thr45Ile
ENST00000468877.2:n.222-10C>T
NM_001190906.1:c.302C>T	NP_001177835.1:p.Thr101Ile
NM_001190907.1:c.302C>T	NP_001177836.1:p.Thr101Ile
NM_005989.3:c.302C>T	NP_005980.1:p.Thr101Ile
NM_005989.4:c.302C>T MANE Select	NP_005980.1:p.Thr101Ile
NM_001190906.2:c.302C>T	NP_001177835.1:p.Thr101Ile
NM_001190907.2:c.302C>T	NP_001177836.1:p.Thr101Ile