Canonical Allele Identifier: CA1932867138

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830907G= , CM000672.2:g.102830907G=	GRCh38
NC_000010.10:g.104590664G= , CM000672.1:g.104590664G=	GRCh37
NC_000010.9:g.104580654G=	NCBI36
NG_007955.1:g.11627C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1322C= (CYP17A1) MANE Select	ENSP00000358903.3:p.Ser441=
ENST00000638190.1:c.1019C= (CYP17A1)	ENSP00000492539.1:p.Ser340=
ENST00000638272.1:c.866C= (CYP17A1)	ENSP00000491508.1:p.Ser289=
ENST00000638971.1:c.1235C= (CYP17A1)	ENSP00000492313.1:p.Ser412=
ENST00000639393.1:c.1325C= (CYP17A1)	ENSP00000492651.1:p.Ser442=
ENST00000640633.1:n.1084C= (CYP17A1)
ENST00000647664.1:c.*589G= (WBP1L)	ENSP00000498131.1:n.*589G=
ENST00000369887.3:c.1322C= (CYP17A1)	ENSP00000358903.3:p.Ser441=
NM_000102.3:c.1322C= (CYP17A1)	NP_000093.1:p.Ser441=
NM_000102.4:c.1322C= (CYP17A1) MANE Select	NP_000093.1:p.Ser441=