Canonical Allele Identifier: CA1932867250

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830957C= , CM000672.2:g.102830957C=	GRCh38
NC_000010.10:g.104590714C= , CM000672.1:g.104590714C=	GRCh37
NC_000010.9:g.104580704C=	NCBI36
NG_007955.1:g.11577G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1272G= (CYP17A1) MANE Select	ENSP00000358903.3:p.Gln424=
ENST00000638190.1:c.969G= (CYP17A1)	ENSP00000492539.1:p.Gln323=
ENST00000638272.1:c.816G= (CYP17A1)	ENSP00000491508.1:p.Gln272=
ENST00000638971.1:c.1185G= (CYP17A1)	ENSP00000492313.1:p.Gln395=
ENST00000639393.1:c.1275G= (CYP17A1)	ENSP00000492651.1:p.Gln425=
ENST00000640633.1:n.1034G= (CYP17A1)
ENST00000647664.1:c.*628+11C= (WBP1L)	ENSP00000498131.1:n.*628+11C=
ENST00000369887.3:c.1272G= (CYP17A1)	ENSP00000358903.3:p.Gln424=
ENST00000469683.1:n.225G= (CYP17A1)
NM_000102.3:c.1272G= (CYP17A1)	NP_000093.1:p.Gln424=
NM_000102.4:c.1272G= (CYP17A1) MANE Select	NP_000093.1:p.Gln424=