Canonical Allele Identifier: CA1932873331

Gene: CYP17A1 WBP1L CYP17A1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102833793T= , CM000672.2:g.102833793T=	GRCh38
NC_000010.10:g.104593550T= , CM000672.1:g.104593550T=	GRCh37
NC_000010.9:g.104583540T=	NCBI36
NG_007955.1:g.8741A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-384T=
ENST00000369887.4:c.753+243A= (CYP17A1) MANE Select	ENSP00000358903.3:n.753+243A=
ENST00000638190.1:c.666+992A= (CYP17A1)	ENSP00000492539.1:n.666+992A=
ENST00000638272.1:c.298-585A= (CYP17A1)	ENSP00000491508.1:n.298-585A=
ENST00000638971.1:c.667-585A= (CYP17A1)	ENSP00000492313.1:n.667-585A=
ENST00000639393.1:c.753+243A= (CYP17A1)	ENSP00000492651.1:n.753+243A=
ENST00000640633.1:n.515+243A= (CYP17A1)
ENST00000647664.1:c.*2824T= (WBP1L)	ENSP00000498131.1:n.*2824T=
ENST00000369887.3:c.753+243A= (CYP17A1)	ENSP00000358903.3:n.753+243A=
ENST00000489268.1:n.1912A= (CYP17A1)
NM_000102.3:c.753+243A= (CYP17A1)	NP_000093.1:n.753+243A=
XR_428804.1:n.206-384T= (CYP17A1-AS1)
NM_000102.4:c.753+243A= (CYP17A1) MANE Select	NP_000093.1:n.753+243A=