Canonical Allele Identifier: CA1107713125
Gene: AKR1D1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138091921_138091929del , CM000669.2:g.138091921_138091929del GRCh38
NC_000007.13:g.137776667_137776675del , CM000669.1:g.137776667_137776675del GRCh37
NC_000007.12:g.137427207_137427215del NCBI36
NG_023342.1:g.20490_20498del

Transcript Alleles

HGVS Amino-acid Change
ENST00000242375.8:c.378+37_378+45del MANE Select ENSP00000242375.3:n.378+37_378+45del
ENST00000242375.7:c.378+37_378+45del ENSP00000242375.3:n.378+37_378+45del
ENST00000411726.6:c.378+37_378+45del ENSP00000402374.2:n.378+37_378+45del
ENST00000432161.5:c.378+37_378+45del ENSP00000389197.1:n.378+37_378+45del
ENST00000438242.1:c.210+37_210+45del ENSP00000397042.1:n.210+37_210+45del
ENST00000468877.2:n.288+37_288+45del
ENST00000470851.1:n.42+37_42+45del
NM_001190906.1:c.378+37_378+45del NP_001177835.1:n.378+37_378+45del
NM_001190907.1:c.378+37_378+45del NP_001177836.1:n.378+37_378+45del
NM_005989.3:c.378+37_378+45del NP_005980.1:n.378+37_378+45del
NM_005989.4:c.378+37_378+45del MANE Select NP_005980.1:n.378+37_378+45del
NM_001190906.2:c.378+37_378+45del NP_001177835.1:n.378+37_378+45del
NM_001190907.2:c.378+37_378+45del NP_001177836.1:n.378+37_378+45del