Canonical Allele Identifier: CA1932873328

Gene: CYP17A1 WBP1L CYP17A1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102833792A= , CM000672.2:g.102833792A=	GRCh38
NC_000010.10:g.104593549A= , CM000672.1:g.104593549A=	GRCh37
NC_000010.9:g.104583539A=	NCBI36
NG_007955.1:g.8742T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-385A=
ENST00000369887.4:c.753+244T= (CYP17A1) MANE Select	ENSP00000358903.3:n.753+244T=
ENST00000638190.1:c.666+993T= (CYP17A1)	ENSP00000492539.1:n.666+993T=
ENST00000638272.1:c.298-584T= (CYP17A1)	ENSP00000491508.1:n.298-584T=
ENST00000638971.1:c.667-584T= (CYP17A1)	ENSP00000492313.1:n.667-584T=
ENST00000639393.1:c.753+244T= (CYP17A1)	ENSP00000492651.1:n.753+244T=
ENST00000640633.1:n.515+244T= (CYP17A1)
ENST00000647664.1:c.*2823A= (WBP1L)	ENSP00000498131.1:n.*2823A=
ENST00000369887.3:c.753+244T= (CYP17A1)	ENSP00000358903.3:n.753+244T=
ENST00000489268.1:n.1913T= (CYP17A1)
NM_000102.3:c.753+244T= (CYP17A1)	NP_000093.1:n.753+244T=
XR_428804.1:n.206-385A= (CYP17A1-AS1)
NM_000102.4:c.753+244T= (CYP17A1) MANE Select	NP_000093.1:n.753+244T=