Canonical Allele Identifier: CA1932870424

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832512T= , CM000672.2:g.102832512T=	GRCh38
NC_000010.10:g.104592269T= , CM000672.1:g.104592269T=	GRCh37
NC_000010.9:g.104582259T=	NCBI36
NG_007955.1:g.10022A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1138A= (CYP17A1) MANE Select	ENSP00000358903.3:p.Ser380=
ENST00000638190.1:c.835A= (CYP17A1)	ENSP00000492539.1:p.Ser279=
ENST00000638272.1:c.682A= (CYP17A1)	ENSP00000491508.1:p.Ser228=
ENST00000638971.1:c.1051A= (CYP17A1)	ENSP00000492313.1:p.Ser351=
ENST00000639393.1:c.1138A= (CYP17A1)	ENSP00000492651.1:p.Ser380=
ENST00000640633.1:n.900A= (CYP17A1)
ENST00000647664.1:c.*1543T= (WBP1L)	ENSP00000498131.1:n.*1543T=
ENST00000369887.3:c.1138A= (CYP17A1)	ENSP00000358903.3:p.Ser380=
NM_000102.3:c.1138A= (CYP17A1)	NP_000093.1:p.Ser380=
NM_000102.4:c.1138A= (CYP17A1) MANE Select	NP_000093.1:p.Ser380=