Canonical Allele Identifier: CA375886171

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5098865T>G , CM000672.2:g.5098865T>G GRCh38
NC_000010.10:g.5141057T>G , CM000672.1:g.5141057T>G GRCh37
NC_000010.9:g.5131057T>G NCBI36
NG_047094.1:g.55100T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000380554.5:c.433T>G (AKR1C3) MANE Select ENSP00000369927.3:p.Cys145Gly
ENST00000380554.4:c.433T>G (AKR1C3) ENSP00000369927.3:p.Cys145Gly
ENST00000407674.5:c.180+33809A>C (AKR1C2) ENSP00000385221.2:n.180+33809A>C
ENST00000434459.6:c.933-8596T>G (AKR1C1) ENSP00000412248.3:n.933-8596T>G
ENST00000439082.7:c.433T>G ENSP00000401327.3:p.Cys145Gly
ENST00000602997.5:c.364T>G (AKR1C3) ENSP00000474188.1:p.Cys122Gly
ENST00000605149.5:c.364T>G (AKR1C3) ENSP00000474882.1:p.Cys122Gly
ENST00000605322.1:n.280-462T>G (AKR1C3)
ENST00000605781.5:n.612T>G (AKR1C3)
NM_001253908.1:c.433T>G (AKR1C3) NP_001240837.1:p.Cys145Gly
NM_003739.5:c.433T>G (AKR1C3) NP_003730.4:p.Cys145Gly
NM_003739.6:c.433T>G (AKR1C3) MANE Select NP_003730.4:p.Cys145Gly
NM_001253908.2:c.433T>G (AKR1C3) NP_001240837.1:p.Cys145Gly