Canonical Allele Identifier: CA5669426

Gene: CYP17A1 WBP1L CYP17A1-AS1

Linked Data

• dbSNP Id: rs768071357
• ExAC: 10:104592434 T / TC
• gnomAD v2: 10-104592434-T-TC
• MyVariant Identifiers: chr10:g.104592434_104592435insC (hg19) ; chr10:g.102832677_102832678insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832678dup , CM000672.2:g.102832678dup	GRCh38
NC_000010.10:g.104592435dup , CM000672.1:g.104592435dup	GRCh37
NC_000010.9:g.104582425dup	NCBI36
NG_007955.1:g.9856dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.972dup (CYP17A1) MANE Select	ENSP00000358903.3:p.Lys325GlufsTer9
ENST00000638190.1:c.669dup (CYP17A1)	ENSP00000492539.1:p.Lys224GlufsTer9
ENST00000638272.1:c.516dup (CYP17A1)	ENSP00000491508.1:p.Lys173GlufsTer9
ENST00000638971.1:c.885dup (CYP17A1)	ENSP00000492313.1:p.Lys296GlufsTer9
ENST00000639393.1:c.972dup (CYP17A1)	ENSP00000492651.1:p.Lys325GlufsTer9
ENST00000640633.1:n.734dup (CYP17A1)
ENST00000647664.1:c.*1709dup (WBP1L)	ENSP00000498131.1:n.*1709dup
ENST00000369887.3:c.972dup (CYP17A1)	ENSP00000358903.3:p.Lys325GlufsTer9
NM_000102.3:c.972dup (CYP17A1)	NP_000093.1:p.Lys325GlufsTer9
XR_428804.1:n.12dup (CYP17A1-AS1)
NM_000102.4:c.972dup (CYP17A1) MANE Select	NP_000093.1:p.Lys325GlufsTer9