Canonical Allele Identifier: CA5669422

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832663G>A , CM000672.2:g.102832663G>A	GRCh38
NC_000010.10:g.104592420G>A , CM000672.1:g.104592420G>A	GRCh37
NC_000010.9:g.104582410G>A	NCBI36
NG_007955.1:g.9871C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000102.4:c.987C>T (CYP17A1) MANE Select	NP_000093.1:p.Tyr329=
ENST00000369887.4:c.987C>T (CYP17A1) MANE Select	ENSP00000358903.3:p.Tyr329=
NM_000102.3:c.987C>T (CYP17A1)	NP_000093.1:p.Tyr329=
ENST00000369887.3:c.987C>T (CYP17A1)	ENSP00000358903.3:p.Tyr329=
ENST00000638190.1:c.684C>T (CYP17A1)	ENSP00000492539.1:p.Tyr228=
ENST00000638272.1:c.531C>T (CYP17A1)	ENSP00000491508.1:p.Tyr177=
ENST00000638971.1:c.900C>T (CYP17A1)	ENSP00000492313.1:p.Tyr300=
ENST00000639393.1:c.987C>T (CYP17A1)	ENSP00000492651.1:p.Tyr329=
ENST00000640633.1:n.749C>T (CYP17A1)
ENST00000647664.1:c.*1694G>A (WBP1L)	ENSP00000498131.1:n.*1694G>A