Canonical Allele Identifier: CA1932868581

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831535A= , CM000672.2:g.102831535A=	GRCh38
NC_000010.10:g.104591292A= , CM000672.1:g.104591292A=	GRCh37
NC_000010.9:g.104581282A=	NCBI36
NG_007955.1:g.10999T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000102.4:c.1216T= (CYP17A1) MANE Select	NP_000093.1:p.Trp406=
ENST00000369887.4:c.1216T= (CYP17A1) MANE Select	ENSP00000358903.3:p.Trp406=
NM_000102.3:c.1216T= (CYP17A1)	NP_000093.1:p.Trp406=
ENST00000369887.3:c.1216T= (CYP17A1)	ENSP00000358903.3:p.Trp406=
ENST00000469683.1:n.169T= (CYP17A1)
ENST00000638190.1:c.913T= (CYP17A1)	ENSP00000492539.1:p.Trp305=
ENST00000638272.1:c.760T= (CYP17A1)	ENSP00000491508.1:p.Trp254=
ENST00000638971.1:c.1129T= (CYP17A1)	ENSP00000492313.1:p.Trp377=
ENST00000639393.1:c.1219T= (CYP17A1)	ENSP00000492651.1:p.Trp407=
ENST00000640633.1:n.978T= (CYP17A1)
ENST00000647664.1:c.*629-63A= (WBP1L)	ENSP00000498131.1:n.*629-63A=