Canonical Allele Identifier: CA457915334
Gene: AKR1D1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.137776555C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138091809C>A , CM000669.2:g.138091809C>A GRCh38
NC_000007.13:g.137776555C>A , CM000669.1:g.137776555C>A GRCh37
NC_000007.12:g.137427095C>A NCBI36
NG_023342.1:g.20378C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000242375.8:c.303C>A MANE Select ENSP00000242375.3:p.Thr101=
ENST00000242375.7:c.303C>A ENSP00000242375.3:p.Thr101=
ENST00000411726.6:c.303C>A ENSP00000402374.2:p.Thr101=
ENST00000432161.5:c.303C>A ENSP00000389197.1:p.Thr101=
ENST00000438242.1:c.135C>A ENSP00000397042.1:p.Thr45=
ENST00000468877.2:n.222-9C>A
NM_001190906.1:c.303C>A NP_001177835.1:p.Thr101=
NM_001190907.1:c.303C>A NP_001177836.1:p.Thr101=
NM_005989.3:c.303C>A NP_005980.1:p.Thr101=
NM_005989.4:c.303C>A MANE Select NP_005980.1:p.Thr101=
NM_001190906.2:c.303C>A NP_001177835.1:p.Thr101=
NM_001190907.2:c.303C>A NP_001177836.1:p.Thr101=