Canonical Allele Identifier: CA1746478255
Gene: AKR1D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138114823A= , CM000669.2:g.138114823A= GRCh38
NC_000007.13:g.137799569A= , CM000669.1:g.137799569A= GRCh37
NC_000007.12:g.137450109A= NCBI36
NG_023342.1:g.43392A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242375.8:c.938+1051A= MANE Select ENSP00000242375.3:n.938+1051A=
ENST00000242375.7:c.938+1051A= ENSP00000242375.3:n.938+1051A=
ENST00000411726.6:c.815+1051A= ENSP00000402374.2:n.815+1051A=
ENST00000432161.5:c.856-1797A= ENSP00000389197.1:n.856-1797A=
ENST00000468877.2:n.961+1051A=
NM_001190906.1:c.815+1051A= NP_001177835.1:n.815+1051A=
NM_001190907.1:c.856-1797A= NP_001177836.1:n.856-1797A=
NM_005989.3:c.938+1051A= NP_005980.1:n.938+1051A=
NM_005989.4:c.938+1051A= MANE Select NP_005980.1:n.938+1051A=
NM_001190906.2:c.815+1051A= NP_001177835.1:n.815+1051A=
NM_001190907.2:c.856-1797A= NP_001177836.1:n.856-1797A=