Canonical Allele Identifier: CA1746468601
Gene: AKR1D1 HGNC NCBI

Linked Data

dbSNP Id: rs1794083636

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138091755T>G , CM000669.2:g.138091755T>G GRCh38
NC_000007.13:g.137776501T>G , CM000669.1:g.137776501T>G GRCh37
NC_000007.12:g.137427041T>G NCBI36
NG_023342.1:g.20324T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000242375.8:c.262-13T>G MANE Select ENSP00000242375.3:n.262-13T>G
ENST00000242375.7:c.262-13T>G ENSP00000242375.3:n.262-13T>G
ENST00000411726.6:c.262-13T>G ENSP00000402374.2:n.262-13T>G
ENST00000432161.5:c.262-13T>G ENSP00000389197.1:n.262-13T>G
ENST00000438242.1:c.94-13T>G ENSP00000397042.1:n.94-13T>G
ENST00000468877.2:n.222-63T>G
NM_001190906.1:c.262-13T>G NP_001177835.1:n.262-13T>G
NM_001190907.1:c.262-13T>G NP_001177836.1:n.262-13T>G
NM_005989.3:c.262-13T>G NP_005980.1:n.262-13T>G
NM_005989.4:c.262-13T>G MANE Select NP_005980.1:n.262-13T>G
NM_001190906.2:c.262-13T>G NP_001177835.1:n.262-13T>G
NM_001190907.2:c.262-13T>G NP_001177836.1:n.262-13T>G