Canonical Allele Identifier: CA202187682

Gene: AKR1C2 AKR1C1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.4991645C>A , CM000672.2:g.4991645C>A	GRCh38
NC_000010.10:g.5033837C>A , CM000672.1:g.5033837C>A	GRCh37
NC_000010.9:g.5023837C>A	NCBI36
NG_031852.1:g.31371G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001393392.1:c.929+186G>T (AKR1C2) MANE Select	NP_001380321.1:n.929+186G>T
ENST00000380753.9:c.929+186G>T (AKR1C2) MANE Select	ENSP00000370129.4:n.929+186G>T
NM_001321027.1:c.851+186G>T (AKR1C2)	NP_001307956.1:n.851+186G>T
NM_001321027.2:c.851+186G>T (AKR1C2)	NP_001307956.1:n.851+186G>T
NM_001354.5:c.929+186G>T (AKR1C2)	NP_001345.1:n.929+186G>T
NM_001354.6:c.929+186G>T (AKR1C2)	NP_001345.1:n.929+186G>T
NM_205845.2:c.929+186G>T (AKR1C2)	NP_995317.1:n.929+186G>T
NM_205845.3:c.929+186G>T (AKR1C2)	NP_995317.1:n.929+186G>T
ENST00000380753.8:c.929+186G>T (AKR1C2)	ENSP00000370129.4:n.929+186G>T
ENST00000407674.5:c.929+186G>T (AKR1C2)	ENSP00000385221.2:n.929+186G>T
ENST00000421196.7:c.851+186G>T (AKR1C2)	ENSP00000392694.2:n.851+186G>T
ENST00000434459.6:c.932+15709C>A (AKR1C1)	ENSP00000412248.3:n.932+15709C>A
ENST00000460124.5:n.2389+186G>T (AKR1C2)
XM_011519342.1:c.851+186G>T (AKR1C2)	XP_011517644.1:n.851+186G>T