Canonical Allele Identifier: CA1932867112

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830896C= , CM000672.2:g.102830896C=	GRCh38
NC_000010.10:g.104590653C= , CM000672.1:g.104590653C=	GRCh37
NC_000010.9:g.104580643C=	NCBI36
NG_007955.1:g.11638G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1333G= (CYP17A1) MANE Select	ENSP00000358903.3:p.Glu445=
ENST00000638190.1:c.1030G= (CYP17A1)	ENSP00000492539.1:p.Glu344=
ENST00000638272.1:c.877G= (CYP17A1)	ENSP00000491508.1:p.Glu293=
ENST00000638971.1:c.1246G= (CYP17A1)	ENSP00000492313.1:p.Glu416=
ENST00000639393.1:c.1336G= (CYP17A1)	ENSP00000492651.1:p.Glu446=
ENST00000640633.1:n.1095G= (CYP17A1)
ENST00000647664.1:c.*578C= (WBP1L)	ENSP00000498131.1:n.*578C=
ENST00000369887.3:c.1333G= (CYP17A1)	ENSP00000358903.3:p.Glu445=
NM_000102.3:c.1333G= (CYP17A1)	NP_000093.1:p.Glu445=
NM_000102.4:c.1333G= (CYP17A1) MANE Select	NP_000093.1:p.Glu445=