Canonical Allele Identifier: CA1932841358

Gene: CYP17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102837302T= , CM000672.2:g.102837302T=	GRCh38
NC_000010.10:g.104597059T= , CM000672.1:g.104597059T=	GRCh37
NC_000010.9:g.104587049T=	NCBI36
NG_007955.1:g.5232A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.60A= MANE Select	ENSP00000358903.3:p.Arg20=
ENST00000638190.1:c.60A=	ENSP00000492539.1:p.Arg20=
ENST00000638272.1:c.60A=	ENSP00000491508.1:p.Arg20=
ENST00000638971.1:c.60A=	ENSP00000492313.1:p.Arg20=
ENST00000639393.1:c.60A=	ENSP00000492651.1:p.Arg20=
ENST00000369887.3:c.60A=	ENSP00000358903.3:p.Arg20=
ENST00000489268.1:n.113A=
NM_000102.3:c.60A=	NP_000093.1:p.Arg20=
NM_000102.4:c.60A= MANE Select	NP_000093.1:p.Arg20=