Canonical Allele Identifier: CA377939007

Gene: CYP17A1 WBP1L CYP17A1-AS1

Linked Data

• ClinVar Variation Id: 2770064
• ClinVar RCV Id: RCV003579012
• MyVariant Identifiers: chr10:g.104592434T>A (hg19) ; chr10:g.102832677T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832677T>A , CM000672.2:g.102832677T>A	GRCh38
NC_000010.10:g.104592434T>A , CM000672.1:g.104592434T>A	GRCh37
NC_000010.9:g.104582424T>A	NCBI36
NG_007955.1:g.9857A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.973A>T (CYP17A1) MANE Select	ENSP00000358903.3:p.Lys325Ter
ENST00000638190.1:c.670A>T (CYP17A1)	ENSP00000492539.1:p.Lys224Ter
ENST00000638272.1:c.517A>T (CYP17A1)	ENSP00000491508.1:p.Lys173Ter
ENST00000638971.1:c.886A>T (CYP17A1)	ENSP00000492313.1:p.Lys296Ter
ENST00000639393.1:c.973A>T (CYP17A1)	ENSP00000492651.1:p.Lys325Ter
ENST00000640633.1:n.735A>T (CYP17A1)
ENST00000647664.1:c.*1708T>A (WBP1L)	ENSP00000498131.1:n.*1708T>A
ENST00000369887.3:c.973A>T (CYP17A1)	ENSP00000358903.3:p.Lys325Ter
NM_000102.3:c.973A>T (CYP17A1)	NP_000093.1:p.Lys325Ter
XR_428804.1:n.11T>A (CYP17A1-AS1)
NM_000102.4:c.973A>T (CYP17A1) MANE Select	NP_000093.1:p.Lys325Ter