Canonical Allele Identifier: CA1932868772

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831621A= , CM000672.2:g.102831621A=	GRCh38
NC_000010.10:g.104591378A= , CM000672.1:g.104591378A=	GRCh37
NC_000010.9:g.104581368A=	NCBI36
NG_007955.1:g.10913T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1140-10T= (CYP17A1) MANE Select	ENSP00000358903.3:n.1140-10T=
ENST00000638190.1:c.837-10T= (CYP17A1)	ENSP00000492539.1:n.837-10T=
ENST00000638272.1:c.684-10T= (CYP17A1)	ENSP00000491508.1:n.684-10T=
ENST00000638971.1:c.1053-10T= (CYP17A1)	ENSP00000492313.1:n.1053-10T=
ENST00000639393.1:c.1140-7T= (CYP17A1)	ENSP00000492651.1:n.1140-7T=
ENST00000640633.1:n.902-10T= (CYP17A1)
ENST00000647664.1:c.*652A= (WBP1L)	ENSP00000498131.1:n.*652A=
ENST00000369887.3:c.1140-10T= (CYP17A1)	ENSP00000358903.3:n.1140-10T=
ENST00000469683.1:n.83T= (CYP17A1)
NM_000102.3:c.1140-10T= (CYP17A1)	NP_000093.1:n.1140-10T=
NM_000102.4:c.1140-10T= (CYP17A1) MANE Select	NP_000093.1:n.1140-10T=