Canonical Allele Identifier: CA595226116

Gene: CYP17A1 WBP1L

Linked Data

• dbSNP Id: rs1417225842
• gnomAD v2: 10-104590654-AC-A
• MyVariant Identifiers: chr10:g.104590655del (hg19) ; chr10:g.102830898del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830899del , CM000672.2:g.102830899del	GRCh38
NC_000010.10:g.104590656del , CM000672.1:g.104590656del	GRCh37
NC_000010.9:g.104580646del	NCBI36
NG_007955.1:g.11636del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1331del (CYP17A1) MANE Select	ENSP00000358903.3:p.Gly444ValfsTer?
ENST00000638190.1:c.1028del (CYP17A1)	ENSP00000492539.1:p.Gly343ValfsTer?
ENST00000638272.1:c.875del (CYP17A1)	ENSP00000491508.1:p.Gly292ValfsTer?
ENST00000638971.1:c.1244del (CYP17A1)	ENSP00000492313.1:p.Gly415ValfsTer?
ENST00000639393.1:c.1334del (CYP17A1)	ENSP00000492651.1:p.Gly445ValfsTer?
ENST00000640633.1:n.1093del (CYP17A1)
ENST00000647664.1:c.*581del (WBP1L)	ENSP00000498131.1:n.*581del
ENST00000369887.3:c.1331del (CYP17A1)	ENSP00000358903.3:p.Gly444ValfsTer?
NM_000102.3:c.1331del (CYP17A1)	NP_000093.1:p.Gly444ValfsTer?
NM_000102.4:c.1331del (CYP17A1) MANE Select	NP_000093.1:p.Gly444ValfsTer?