Canonical Allele Identifier: CA1932870038

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832369G= , CM000672.2:g.102832369G=	GRCh38
NC_000010.10:g.104592126G= , CM000672.1:g.104592126G=	GRCh37
NC_000010.9:g.104582116G=	NCBI36
NG_007955.1:g.10165C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1139+142C= (CYP17A1) MANE Select	ENSP00000358903.3:n.1139+142C=
ENST00000638190.1:c.836+142C= (CYP17A1)	ENSP00000492539.1:n.836+142C=
ENST00000638272.1:c.683+142C= (CYP17A1)	ENSP00000491508.1:n.683+142C=
ENST00000638971.1:c.1052+142C= (CYP17A1)	ENSP00000492313.1:n.1052+142C=
ENST00000639393.1:c.1139+142C= (CYP17A1)	ENSP00000492651.1:n.1139+142C=
ENST00000640633.1:n.901+142C= (CYP17A1)
ENST00000647664.1:c.*1400G= (WBP1L)	ENSP00000498131.1:n.*1400G=
ENST00000369887.3:c.1139+142C= (CYP17A1)	ENSP00000358903.3:n.1139+142C=
NM_000102.3:c.1139+142C= (CYP17A1)	NP_000093.1:n.1139+142C=
NM_000102.4:c.1139+142C= (CYP17A1) MANE Select	NP_000093.1:n.1139+142C=