Canonical Allele Identifier: CA1932840756

Gene: CYP17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102836699A= , CM000672.2:g.102836699A=	GRCh38
NC_000010.10:g.104596456A= , CM000672.1:g.104596456A=	GRCh37
NC_000010.9:g.104586446A=	NCBI36
NG_007955.1:g.5835T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.297+366T= MANE Select	ENSP00000358903.3:n.297+366T=
ENST00000638190.1:c.297+366T=	ENSP00000492539.1:n.297+366T=
ENST00000638272.1:c.297+366T=	ENSP00000491508.1:n.297+366T=
ENST00000638971.1:c.297+366T=	ENSP00000492313.1:n.297+366T=
ENST00000639393.1:c.297+366T=	ENSP00000492651.1:n.297+366T=
ENST00000640633.1:n.59+15T=
ENST00000369887.3:c.297+366T=	ENSP00000358903.3:n.297+366T=
ENST00000489268.1:n.350+366T=
NM_000102.3:c.297+366T=	NP_000093.1:n.297+366T=
NM_000102.4:c.297+366T= MANE Select	NP_000093.1:n.297+366T=