Canonical Allele Identifier: CA1932867223

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830946G= , CM000672.2:g.102830946G=	GRCh38
NC_000010.10:g.104590703G= , CM000672.1:g.104590703G=	GRCh37
NC_000010.9:g.104580693G=	NCBI36
NG_007955.1:g.11588C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000102.4:c.1283C= (CYP17A1) MANE Select	NP_000093.1:p.Pro428=
ENST00000369887.4:c.1283C= (CYP17A1) MANE Select	ENSP00000358903.3:p.Pro428=
NM_000102.3:c.1283C= (CYP17A1)	NP_000093.1:p.Pro428=
ENST00000369887.3:c.1283C= (CYP17A1)	ENSP00000358903.3:p.Pro428=
ENST00000638190.1:c.980C= (CYP17A1)	ENSP00000492539.1:p.Pro327=
ENST00000638272.1:c.827C= (CYP17A1)	ENSP00000491508.1:p.Pro276=
ENST00000638971.1:c.1196C= (CYP17A1)	ENSP00000492313.1:p.Pro399=
ENST00000639393.1:c.1286C= (CYP17A1)	ENSP00000492651.1:p.Pro429=
ENST00000640633.1:n.1045C= (CYP17A1)
ENST00000647664.1:c.*628G= (WBP1L)	ENSP00000498131.1:n.*628G=