Canonical Allele Identifier: CA1932867211

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830945C= , CM000672.2:g.102830945C=	GRCh38
NC_000010.10:g.104590702C= , CM000672.1:g.104590702C=	GRCh37
NC_000010.9:g.104580692C=	NCBI36
NG_007955.1:g.11589G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1284G= (CYP17A1) MANE Select	ENSP00000358903.3:p.Pro428=
ENST00000638190.1:c.981G= (CYP17A1)	ENSP00000492539.1:p.Pro327=
ENST00000638272.1:c.828G= (CYP17A1)	ENSP00000491508.1:p.Pro276=
ENST00000638971.1:c.1197G= (CYP17A1)	ENSP00000492313.1:p.Pro399=
ENST00000639393.1:c.1287G= (CYP17A1)	ENSP00000492651.1:p.Pro429=
ENST00000640633.1:n.1046G= (CYP17A1)
ENST00000647664.1:c.*627C= (WBP1L)	ENSP00000498131.1:n.*627C=
ENST00000369887.3:c.1284G= (CYP17A1)	ENSP00000358903.3:p.Pro428=
NM_000102.3:c.1284G= (CYP17A1)	NP_000093.1:p.Pro428=
NM_000102.4:c.1284G= (CYP17A1) MANE Select	NP_000093.1:p.Pro428=