Canonical Allele Identifier: CA1932866922

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830858G= , CM000672.2:g.102830858G=	GRCh38
NC_000010.10:g.104590615G= , CM000672.1:g.104590615G=	GRCh37
NC_000010.9:g.104580605G=	NCBI36
NG_007955.1:g.11676C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1371C= (CYP17A1) MANE Select	ENSP00000358903.3:p.Ala457=
ENST00000638190.1:c.1068C= (CYP17A1)	ENSP00000492539.1:p.Ala356=
ENST00000638272.1:c.915C= (CYP17A1)	ENSP00000491508.1:p.Ala305=
ENST00000638971.1:c.1284C= (CYP17A1)	ENSP00000492313.1:p.Ala428=
ENST00000639393.1:c.1374C= (CYP17A1)	ENSP00000492651.1:p.Ala458=
ENST00000640633.1:n.1133C= (CYP17A1)
ENST00000647664.1:c.*540G= (WBP1L)	ENSP00000498131.1:n.*540G=
ENST00000369887.3:c.1371C= (CYP17A1)	ENSP00000358903.3:p.Ala457=
NM_000102.3:c.1371C= (CYP17A1)	NP_000093.1:p.Ala457=
NM_000102.4:c.1371C= (CYP17A1) MANE Select	NP_000093.1:p.Ala457=