Canonical Allele Identifier: CA156198
Community Standard Title: NM_003739.6(AKR1C3):c.643G>A (p.Ala215Thr)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5102173G>A , CM000672.2:g.5102173G>A GRCh38
NC_000010.10:g.5144365G>A , CM000672.1:g.5144365G>A GRCh37
NC_000010.9:g.5134365G>A NCBI36
NG_047094.1:g.58408G>A

Transcript Alleles

HGVS Amino-acid Change
NM_003739.6:c.643G>A (AKR1C3) MANE Select NP_003730.4:p.Ala215Thr
ENST00000380554.5:c.643G>A (AKR1C3) MANE Select ENSP00000369927.3:p.Ala215Thr
NM_001253908.1:c.643G>A (AKR1C3) NP_001240837.1:p.Ala215Thr
NM_001253908.2:c.643G>A (AKR1C3) NP_001240837.1:p.Ala215Thr
NM_003739.5:c.643G>A (AKR1C3) NP_003730.4:p.Ala215Thr
ENST00000380554.4:c.643G>A (AKR1C3) ENSP00000369927.3:p.Ala215Thr
ENST00000407674.5:c.180+30501C>T (AKR1C2) ENSP00000385221.2:n.180+30501C>T
ENST00000434459.6:c.933-5288G>A (AKR1C1) ENSP00000412248.3:n.933-5288G>A
ENST00000439082.7:c.643G>A ENSP00000401327.3:p.Ala215Thr
ENST00000605149.5:c.574G>A (AKR1C3) ENSP00000474882.1:p.Ala192Thr
ENST00000605781.5:n.822G>A (AKR1C3)