Canonical Allele Identifier: CA1932841354

Gene: CYP17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102837298A= , CM000672.2:g.102837298A=	GRCh38
NC_000010.10:g.104597055A= , CM000672.1:g.104597055A=	GRCh37
NC_000010.9:g.104587045A=	NCBI36
NG_007955.1:g.5236T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.64T= MANE Select	ENSP00000358903.3:p.Cys22=
ENST00000638190.1:c.64T=	ENSP00000492539.1:p.Cys22=
ENST00000638272.1:c.64T=	ENSP00000491508.1:p.Cys22=
ENST00000638971.1:c.64T=	ENSP00000492313.1:p.Cys22=
ENST00000639393.1:c.64T=	ENSP00000492651.1:p.Cys22=
ENST00000369887.3:c.64T=	ENSP00000358903.3:p.Cys22=
ENST00000489268.1:n.117T=
NM_000102.3:c.64T=	NP_000093.1:p.Cys22=
NM_000102.4:c.64T= MANE Select	NP_000093.1:p.Cys22=