Canonical Allele Identifier: CA1932867178

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830922C= , CM000672.2:g.102830922C=	GRCh38
NC_000010.10:g.104590679C= , CM000672.1:g.104590679C=	GRCh37
NC_000010.9:g.104580669C=	NCBI36
NG_007955.1:g.11612G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1307G= (CYP17A1) MANE Select	ENSP00000358903.3:p.Gly436=
ENST00000638190.1:c.1004G= (CYP17A1)	ENSP00000492539.1:p.Gly335=
ENST00000638272.1:c.851G= (CYP17A1)	ENSP00000491508.1:p.Gly284=
ENST00000638971.1:c.1220G= (CYP17A1)	ENSP00000492313.1:p.Gly407=
ENST00000639393.1:c.1310G= (CYP17A1)	ENSP00000492651.1:p.Gly437=
ENST00000640633.1:n.1069G= (CYP17A1)
ENST00000647664.1:c.*604C= (WBP1L)	ENSP00000498131.1:n.*604C=
ENST00000369887.3:c.1307G= (CYP17A1)	ENSP00000358903.3:p.Gly436=
NM_000102.3:c.1307G= (CYP17A1)	NP_000093.1:p.Gly436=
NM_000102.4:c.1307G= (CYP17A1) MANE Select	NP_000093.1:p.Gly436=