Canonical Allele Identifier: CA2610723242

Gene: CYP17A1 WBP1L

Linked Data

• gnomAD v4: 10-102832532-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832537del , CM000672.2:g.102832537del	GRCh38
NC_000010.10:g.104592294del , CM000672.1:g.104592294del	GRCh37
NC_000010.9:g.104582284del	NCBI36
NG_007955.1:g.10001del

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1117del (CYP17A1) MANE Select	ENSP00000358903.3:p.His373ThrfsTer?
ENST00000638190.1:c.814del (CYP17A1)	ENSP00000492539.1:p.His272ThrfsTer?
ENST00000638272.1:c.661del (CYP17A1)	ENSP00000491508.1:p.His221ThrfsTer?
ENST00000638971.1:c.1030del (CYP17A1)	ENSP00000492313.1:p.His344ThrfsTer?
ENST00000639393.1:c.1117del (CYP17A1)	ENSP00000492651.1:p.His373ThrfsTer?
ENST00000640633.1:n.879del (CYP17A1)
ENST00000647664.1:c.*1568del (WBP1L)	ENSP00000498131.1:n.*1568del
ENST00000369887.3:c.1117del (CYP17A1)	ENSP00000358903.3:p.His373ThrfsTer?
NM_000102.3:c.1117del (CYP17A1)	NP_000093.1:p.His373ThrfsTer?
NM_000102.4:c.1117del (CYP17A1) MANE Select	NP_000093.1:p.His373ThrfsTer?