Canonical Allele Identifier: CA471288771

Gene: CYP17A1 WBP1L

Linked Data

• ClinVar Variation Id: 1146733
• ClinVar RCV Id: RCV001486030
• dbSNP Id: rs771526981
• MyVariant Identifiers: chr10:g.104592411A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832654A>T , CM000672.2:g.102832654A>T	GRCh38
NC_000010.10:g.104592411A>T , CM000672.1:g.104592411A>T	GRCh37
NC_000010.9:g.104582401A>T	NCBI36
NG_007955.1:g.9880T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.996T>A (CYP17A1) MANE Select	ENSP00000358903.3:p.Ile332=
ENST00000638190.1:c.693T>A (CYP17A1)	ENSP00000492539.1:p.Ile231=
ENST00000638272.1:c.540T>A (CYP17A1)	ENSP00000491508.1:p.Ile180=
ENST00000638971.1:c.909T>A (CYP17A1)	ENSP00000492313.1:p.Ile303=
ENST00000639393.1:c.996T>A (CYP17A1)	ENSP00000492651.1:p.Ile332=
ENST00000640633.1:n.758T>A (CYP17A1)
ENST00000647664.1:c.*1685A>T (WBP1L)	ENSP00000498131.1:n.*1685A>T
ENST00000369887.3:c.996T>A (CYP17A1)	ENSP00000358903.3:p.Ile332=
NM_000102.3:c.996T>A (CYP17A1)	NP_000093.1:p.Ile332=
NM_000102.4:c.996T>A (CYP17A1) MANE Select	NP_000093.1:p.Ile332=