Canonical Allele Identifier: CA1887557923

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5098857T= , CM000672.2:g.5098857T= GRCh38
NC_000010.10:g.5141049T= , CM000672.1:g.5141049T= GRCh37
NC_000010.9:g.5131049T= NCBI36
NG_047094.1:g.55092T=

Transcript Alleles

HGVS Amino-acid change
ENST00000380554.5:c.425T= (AKR1C3) MANE Select ENSP00000369927.3:p.Val142=
ENST00000380554.4:c.425T= (AKR1C3) ENSP00000369927.3:p.Val142=
ENST00000407674.5:c.180+33817A= (AKR1C2) ENSP00000385221.2:n.180+33817A=
ENST00000434459.6:c.933-8604T= (AKR1C1) ENSP00000412248.3:n.933-8604T=
ENST00000439082.7:c.425T= ENSP00000401327.3:p.Val142=
ENST00000602997.5:c.356T= (AKR1C3) ENSP00000474188.1:p.Val119=
ENST00000605149.5:c.356T= (AKR1C3) ENSP00000474882.1:p.Val119=
ENST00000605322.1:n.280-470T= (AKR1C3)
ENST00000605781.5:n.604T= (AKR1C3)
NM_001253908.1:c.425T= (AKR1C3) NP_001240837.1:p.Val142=
NM_003739.5:c.425T= (AKR1C3) NP_003730.4:p.Val142=
NM_003739.6:c.425T= (AKR1C3) MANE Select NP_003730.4:p.Val142=
NM_001253908.2:c.425T= (AKR1C3) NP_001240837.1:p.Val142=