Canonical Allele Identifier: CA1932868497

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831513A= , CM000672.2:g.102831513A=	GRCh38
NC_000010.10:g.104591270A= , CM000672.1:g.104591270A=	GRCh37
NC_000010.9:g.104581260A=	NCBI36
NG_007955.1:g.11021T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1238T= (CYP17A1) MANE Select	ENSP00000358903.3:p.Met413=
ENST00000638190.1:c.935T= (CYP17A1)	ENSP00000492539.1:p.Met312=
ENST00000638272.1:c.782T= (CYP17A1)	ENSP00000491508.1:p.Met261=
ENST00000638971.1:c.1151T= (CYP17A1)	ENSP00000492313.1:p.Met384=
ENST00000639393.1:c.1241T= (CYP17A1)	ENSP00000492651.1:p.Met414=
ENST00000640633.1:n.1000T= (CYP17A1)
ENST00000647664.1:c.*629-85A= (WBP1L)	ENSP00000498131.1:n.*629-85A=
ENST00000369887.3:c.1238T= (CYP17A1)	ENSP00000358903.3:p.Met413=
ENST00000469683.1:n.191T= (CYP17A1)
NM_000102.3:c.1238T= (CYP17A1)	NP_000093.1:p.Met413=
NM_000102.4:c.1238T= (CYP17A1) MANE Select	NP_000093.1:p.Met413=