Canonical Allele Identifier: CA5669372

Gene: CYP17A1 WBP1L

Linked Data

• dbSNP Id: rs376049925
• ExAC: 10:104591293 C / T
• gnomAD v2: 10-104591293-C-T
• MyVariant Identifiers: chr10:g.104591293C>T (hg19) ; chr10:g.102831536C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831536C>T , CM000672.2:g.102831536C>T	GRCh38
NC_000010.10:g.104591293C>T , CM000672.1:g.104591293C>T	GRCh37
NC_000010.9:g.104581283C>T	NCBI36
NG_007955.1:g.10998G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1215G>A (CYP17A1) MANE Select	ENSP00000358903.3:p.Glu405=
ENST00000638190.1:c.912G>A (CYP17A1)	ENSP00000492539.1:p.Glu304=
ENST00000638272.1:c.759G>A (CYP17A1)	ENSP00000491508.1:p.Glu253=
ENST00000638971.1:c.1128G>A (CYP17A1)	ENSP00000492313.1:p.Glu376=
ENST00000639393.1:c.1218G>A (CYP17A1)	ENSP00000492651.1:p.Glu406=
ENST00000640633.1:n.977G>A (CYP17A1)
ENST00000647664.1:c.*629-62C>T (WBP1L)	ENSP00000498131.1:n.*629-62C>T
ENST00000369887.3:c.1215G>A (CYP17A1)	ENSP00000358903.3:p.Glu405=
ENST00000469683.1:n.168G>A (CYP17A1)
NM_000102.3:c.1215G>A (CYP17A1)	NP_000093.1:p.Glu405=
NM_000102.4:c.1215G>A (CYP17A1) MANE Select	NP_000093.1:p.Glu405=