Canonical Allele Identifier: CA1932839594

Gene: CYP17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835305T= , CM000672.2:g.102835305T=	GRCh38
NC_000010.10:g.104595062T= , CM000672.1:g.104595062T=	GRCh37
NC_000010.9:g.104585052T=	NCBI36
NG_007955.1:g.7229A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.385A= MANE Select	ENSP00000358903.3:p.Met129=
ENST00000638190.1:c.385A=	ENSP00000492539.1:p.Met129=
ENST00000638272.1:c.297+1760A=	ENSP00000491508.1:n.297+1760A=
ENST00000638971.1:c.385A=	ENSP00000492313.1:p.Met129=
ENST00000639393.1:c.385A=	ENSP00000492651.1:p.Met129=
ENST00000640633.1:n.147A=
ENST00000369887.3:c.385A=	ENSP00000358903.3:p.Met129=
ENST00000489268.1:n.639A=
NM_000102.3:c.385A=	NP_000093.1:p.Met129=
NM_000102.4:c.385A= MANE Select	NP_000093.1:p.Met129=