Canonical Allele Identifier: CA1887557928

Gene: AKR1C3 AKR1C2 AKR1C1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.5098863T= , CM000672.2:g.5098863T=	GRCh38
NC_000010.10:g.5141055T= , CM000672.1:g.5141055T=	GRCh37
NC_000010.9:g.5131055T=	NCBI36
NG_047094.1:g.55098T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380554.5:c.431T= (AKR1C3) MANE Select	ENSP00000369927.3:p.Leu144=
ENST00000380554.4:c.431T= (AKR1C3)	ENSP00000369927.3:p.Leu144=
ENST00000407674.5:c.180+33811A= (AKR1C2)	ENSP00000385221.2:n.180+33811A=
ENST00000434459.6:c.933-8598T= (AKR1C1)	ENSP00000412248.3:n.933-8598T=
ENST00000439082.7:c.431T=	ENSP00000401327.3:p.Leu144=
ENST00000602997.5:c.362T= (AKR1C3)	ENSP00000474188.1:p.Leu121=
ENST00000605149.5:c.362T= (AKR1C3)	ENSP00000474882.1:p.Leu121=
ENST00000605322.1:n.280-464T= (AKR1C3)
ENST00000605781.5:n.610T= (AKR1C3)
NM_001253908.1:c.431T= (AKR1C3)	NP_001240837.1:p.Leu144=
NM_003739.5:c.431T= (AKR1C3)	NP_003730.4:p.Leu144=
NM_003739.6:c.431T= (AKR1C3) MANE Select	NP_003730.4:p.Leu144=
NM_001253908.2:c.431T= (AKR1C3)	NP_001240837.1:p.Leu144=