Canonical Allele Identifier: CA202186252
Gene: AKR1C2 HGNC NCBI
AKR1C1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.4989699G>T , CM000672.2:g.4989699G>T GRCh38
NC_000010.10:g.5031891G>T , CM000672.1:g.5031891G>T GRCh37
NC_000010.9:g.5021891G>T NCBI36
NG_031852.1:g.33317C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000380753.9:c.*297C>A (AKR1C2) MANE Select ENSP00000370129.4:n.*297C>A
ENST00000380753.8:c.*297C>A (AKR1C2) ENSP00000370129.4:n.*297C>A
ENST00000407674.5:c.929+2132C>A (AKR1C2) ENSP00000385221.2:n.929+2132C>A
ENST00000421196.7:c.*297C>A (AKR1C2) ENSP00000392694.2:n.*297C>A
ENST00000434459.6:c.932+13763G>T (AKR1C1) ENSP00000412248.3:n.932+13763G>T
NM_001354.5:c.*297C>A (AKR1C2) NP_001345.1:n.*297C>A
NM_205845.2:c.*297C>A (AKR1C2) NP_995317.1:n.*297C>A
NM_001321027.1:c.*297C>A (AKR1C2) NP_001307956.1:n.*297C>A
NM_001321027.2:c.*297C>A (AKR1C2) NP_001307956.1:n.*297C>A
NM_001354.6:c.*297C>A (AKR1C2) NP_001345.1:n.*297C>A
NM_001393392.1:c.*297C>A (AKR1C2) MANE Select NP_001380321.1:n.*297C>A
NM_205845.3:c.*297C>A (AKR1C2) NP_995317.1:n.*297C>A