Canonical Allele Identifier: CA1887558014

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5099002G= , CM000672.2:g.5099002G= GRCh38
NC_000010.10:g.5141194G= , CM000672.1:g.5141194G= GRCh37
NC_000010.9:g.5131194G= NCBI36
NG_047094.1:g.55237G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380554.5:c.447+123G= (AKR1C3) MANE Select ENSP00000369927.3:n.447+123G=
ENST00000380554.4:c.447+123G= (AKR1C3) ENSP00000369927.3:n.447+123G=
ENST00000407674.5:c.180+33672C= (AKR1C2) ENSP00000385221.2:n.180+33672C=
ENST00000434459.6:c.933-8459G= (AKR1C1) ENSP00000412248.3:n.933-8459G=
ENST00000439082.7:c.447+123G= ENSP00000401327.3:n.447+123G=
ENST00000602997.5:c.378+123G= (AKR1C3) ENSP00000474188.1:n.378+123G=
ENST00000605149.5:c.378+123G= (AKR1C3) ENSP00000474882.1:n.378+123G=
ENST00000605322.1:n.280-325G= (AKR1C3)
ENST00000605781.5:n.626+123G= (AKR1C3)
NM_001253908.1:c.447+123G= (AKR1C3) NP_001240837.1:n.447+123G=
NM_003739.5:c.447+123G= (AKR1C3) NP_003730.4:n.447+123G=
NM_003739.6:c.447+123G= (AKR1C3) MANE Select NP_003730.4:n.447+123G=
NM_001253908.2:c.447+123G= (AKR1C3) NP_001240837.1:n.447+123G=