Canonical Allele Identifier: CA1887558030

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5099031C= , CM000672.2:g.5099031C= GRCh38
NC_000010.10:g.5141223C= , CM000672.1:g.5141223C= GRCh37
NC_000010.9:g.5131223C= NCBI36
NG_047094.1:g.55266C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380554.5:c.447+152C= (AKR1C3) MANE Select ENSP00000369927.3:n.447+152C=
ENST00000380554.4:c.447+152C= (AKR1C3) ENSP00000369927.3:n.447+152C=
ENST00000407674.5:c.180+33643G= (AKR1C2) ENSP00000385221.2:n.180+33643G=
ENST00000434459.6:c.933-8430C= (AKR1C1) ENSP00000412248.3:n.933-8430C=
ENST00000439082.7:c.447+152C= ENSP00000401327.3:n.447+152C=
ENST00000602997.5:c.378+152C= (AKR1C3) ENSP00000474188.1:n.378+152C=
ENST00000605149.5:c.378+152C= (AKR1C3) ENSP00000474882.1:n.378+152C=
ENST00000605322.1:n.280-296C= (AKR1C3)
ENST00000605781.5:n.626+152C= (AKR1C3)
NM_001253908.1:c.447+152C= (AKR1C3) NP_001240837.1:n.447+152C=
NM_003739.5:c.447+152C= (AKR1C3) NP_003730.4:n.447+152C=
NM_003739.6:c.447+152C= (AKR1C3) MANE Select NP_003730.4:n.447+152C=
NM_001253908.2:c.447+152C= (AKR1C3) NP_001240837.1:n.447+152C=