Canonical Allele Identifier: CA1887555278

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5093956A= , CM000672.2:g.5093956A= GRCh38
NC_000010.10:g.5136148A= , CM000672.1:g.5136148A= GRCh37
NC_000010.9:g.5126148A= NCBI36
NG_047094.1:g.50191A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380554.4:c.-489A= (AKR1C3) ENSP00000369927.3:n.-489A=
ENST00000407674.5:c.180+38718T= (AKR1C2) ENSP00000385221.2:n.180+38718T=
ENST00000434459.6:c.933-13505A= (AKR1C1) ENSP00000412248.3:n.933-13505A=
ENST00000439082.7:c.85-2454A= ENSP00000401327.3:n.85-2454A=
ENST00000470862.6:n.729-2454A= (AKR1C3)
ENST00000480822.5:n.524-2454A= (AKR1C3)
ENST00000602997.5:c.16-2454A= (AKR1C3) ENSP00000474188.1:n.16-2454A=
ENST00000605149.5:c.16-2454A= (AKR1C3) ENSP00000474882.1:n.16-2454A=
ENST00000605781.5:n.264-2454A= (AKR1C3)
NM_001253908.1:c.85-2454A= (AKR1C3) NP_001240837.1:n.85-2454A=
NM_001253908.2:c.85-2454A= (AKR1C3) NP_001240837.1:n.85-2454A=