Canonical Allele Identifier: CA1932866938

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830863T= , CM000672.2:g.102830863T=	GRCh38
NC_000010.10:g.104590620T= , CM000672.1:g.104590620T=	GRCh37
NC_000010.9:g.104580610T=	NCBI36
NG_007955.1:g.11671A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1366A= (CYP17A1) MANE Select	ENSP00000358903.3:p.Met456=
ENST00000638190.1:c.1063A= (CYP17A1)	ENSP00000492539.1:p.Met355=
ENST00000638272.1:c.910A= (CYP17A1)	ENSP00000491508.1:p.Met304=
ENST00000638971.1:c.1279A= (CYP17A1)	ENSP00000492313.1:p.Met427=
ENST00000639393.1:c.1369A= (CYP17A1)	ENSP00000492651.1:p.Met457=
ENST00000640633.1:n.1128A= (CYP17A1)
ENST00000647664.1:c.*545T= (WBP1L)	ENSP00000498131.1:n.*545T=
ENST00000369887.3:c.1366A= (CYP17A1)	ENSP00000358903.3:p.Met456=
NM_000102.3:c.1366A= (CYP17A1)	NP_000093.1:p.Met456=
NM_000102.4:c.1366A= (CYP17A1) MANE Select	NP_000093.1:p.Met456=