Canonical Allele Identifier: CA1887558010
Gene: AKR1C3 HGNC NCBI
AKR1C2 HGNC NCBI
AKR1C1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5098991A= , CM000672.2:g.5098991A= GRCh38
NC_000010.10:g.5141183A= , CM000672.1:g.5141183A= GRCh37
NC_000010.9:g.5131183A= NCBI36
NG_047094.1:g.55226A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380554.5:c.447+112A= (AKR1C3) MANE Select ENSP00000369927.3:n.447+112A=
ENST00000380554.4:c.447+112A= (AKR1C3) ENSP00000369927.3:n.447+112A=
ENST00000407674.5:c.180+33683T= (AKR1C2) ENSP00000385221.2:n.180+33683T=
ENST00000434459.6:c.933-8470A= (AKR1C1) ENSP00000412248.3:n.933-8470A=
ENST00000439082.7:c.447+112A= ENSP00000401327.3:n.447+112A=
ENST00000602997.5:c.378+112A= (AKR1C3) ENSP00000474188.1:n.378+112A=
ENST00000605149.5:c.378+112A= (AKR1C3) ENSP00000474882.1:n.378+112A=
ENST00000605322.1:n.280-336A= (AKR1C3)
ENST00000605781.5:n.626+112A= (AKR1C3)
NM_001253908.1:c.447+112A= (AKR1C3) NP_001240837.1:n.447+112A=
NM_003739.5:c.447+112A= (AKR1C3) NP_003730.4:n.447+112A=
NM_003739.6:c.447+112A= (AKR1C3) MANE Select NP_003730.4:n.447+112A=
NM_001253908.2:c.447+112A= (AKR1C3) NP_001240837.1:n.447+112A=
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