Canonical Allele Identifier: CA457915367
Gene: AKR1D1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.137776583C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138091837C>T , CM000669.2:g.138091837C>T GRCh38
NC_000007.13:g.137776583C>T , CM000669.1:g.137776583C>T GRCh37
NC_000007.12:g.137427123C>T NCBI36
NG_023342.1:g.20406C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000242375.8:c.331C>T MANE Select ENSP00000242375.3:p.Leu111=
ENST00000242375.7:c.331C>T ENSP00000242375.3:p.Leu111=
ENST00000411726.6:c.331C>T ENSP00000402374.2:p.Leu111=
ENST00000432161.5:c.331C>T ENSP00000389197.1:p.Leu111=
ENST00000438242.1:c.163C>T ENSP00000397042.1:p.Leu55=
ENST00000468877.2:n.241C>T
NM_001190906.1:c.331C>T NP_001177835.1:p.Leu111=
NM_001190907.1:c.331C>T NP_001177836.1:p.Leu111=
NM_005989.3:c.331C>T NP_005980.1:p.Leu111=
NM_005989.4:c.331C>T MANE Select NP_005980.1:p.Leu111=
NM_001190906.2:c.331C>T NP_001177835.1:p.Leu111=
NM_001190907.2:c.331C>T NP_001177836.1:p.Leu111=