Canonical Allele Identifier: CA457915399
Gene: AKR1D1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.137776594G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138091848G>T , CM000669.2:g.138091848G>T GRCh38
NC_000007.13:g.137776594G>T , CM000669.1:g.137776594G>T GRCh37
NC_000007.12:g.137427134G>T NCBI36
NG_023342.1:g.20417G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000242375.8:c.342G>T MANE Select ENSP00000242375.3:p.Val114=
ENST00000242375.7:c.342G>T ENSP00000242375.3:p.Val114=
ENST00000411726.6:c.342G>T ENSP00000402374.2:p.Val114=
ENST00000432161.5:c.342G>T ENSP00000389197.1:p.Val114=
ENST00000438242.1:c.174G>T ENSP00000397042.1:p.Val58=
ENST00000468877.2:n.252G>T
ENST00000470851.1:n.6G>T
NM_001190906.1:c.342G>T NP_001177835.1:p.Val114=
NM_001190907.1:c.342G>T NP_001177836.1:p.Val114=
NM_005989.3:c.342G>T NP_005980.1:p.Val114=
NM_005989.4:c.342G>T MANE Select NP_005980.1:p.Val114=
NM_001190906.2:c.342G>T NP_001177835.1:p.Val114=
NM_001190907.2:c.342G>T NP_001177836.1:p.Val114=