Canonical Allele Identifier: CA1887557988
Community Standard Title: NM_003739.6(AKR1C3):c.447+66A=

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5098945A= , CM000672.2:g.5098945A= GRCh38
NC_000010.10:g.5141137A= , CM000672.1:g.5141137A= GRCh37
NC_000010.9:g.5131137A= NCBI36
NG_047094.1:g.55180A=

Transcript Alleles

HGVS Amino-acid Change
NM_003739.6:c.447+66A= (AKR1C3) MANE Select NP_003730.4:n.447+66A=
ENST00000380554.5:c.447+66A= (AKR1C3) MANE Select ENSP00000369927.3:n.447+66A=
NM_001253908.1:c.447+66A= (AKR1C3) NP_001240837.1:n.447+66A=
NM_001253908.2:c.447+66A= (AKR1C3) NP_001240837.1:n.447+66A=
NM_003739.5:c.447+66A= (AKR1C3) NP_003730.4:n.447+66A=
ENST00000380554.4:c.447+66A= (AKR1C3) ENSP00000369927.3:n.447+66A=
ENST00000407674.5:c.180+33729T= (AKR1C2) ENSP00000385221.2:n.180+33729T=
ENST00000434459.6:c.933-8516A= (AKR1C1) ENSP00000412248.3:n.933-8516A=
ENST00000439082.7:c.447+66A= ENSP00000401327.3:n.447+66A=
ENST00000602997.5:c.378+66A= (AKR1C3) ENSP00000474188.1:n.378+66A=
ENST00000605149.5:c.378+66A= (AKR1C3) ENSP00000474882.1:n.378+66A=
ENST00000605322.1:n.280-382A= (AKR1C3)
ENST00000605781.5:n.626+66A= (AKR1C3)