Canonical Allele Identifier: CA1887557876

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5098763T= , CM000672.2:g.5098763T= GRCh38
NC_000010.10:g.5140955T= , CM000672.1:g.5140955T= GRCh37
NC_000010.9:g.5130955T= NCBI36
NG_047094.1:g.54998T=

Transcript Alleles

HGVS Amino-acid change
ENST00000380554.5:c.370-39T= (AKR1C3) MANE Select ENSP00000369927.3:n.370-39T=
ENST00000380554.4:c.370-39T= (AKR1C3) ENSP00000369927.3:n.370-39T=
ENST00000407674.5:c.180+33911A= (AKR1C2) ENSP00000385221.2:n.180+33911A=
ENST00000434459.6:c.933-8698T= (AKR1C1) ENSP00000412248.3:n.933-8698T=
ENST00000439082.7:c.370-39T= ENSP00000401327.3:n.370-39T=
ENST00000602997.5:c.301-39T= (AKR1C3) ENSP00000474188.1:n.301-39T=
ENST00000605149.5:c.301-39T= (AKR1C3) ENSP00000474882.1:n.301-39T=
ENST00000605322.1:n.280-564T= (AKR1C3)
ENST00000605781.5:n.549-39T= (AKR1C3)
NM_001253908.1:c.370-39T= (AKR1C3) NP_001240837.1:n.370-39T=
NM_003739.5:c.370-39T= (AKR1C3) NP_003730.4:n.370-39T=
NM_003739.6:c.370-39T= (AKR1C3) MANE Select NP_003730.4:n.370-39T=
NM_001253908.2:c.370-39T= (AKR1C3) NP_001240837.1:n.370-39T=