Canonical Allele Identifier: CA2610723241

Gene: CYP17A1 WBP1L

Linked Data

• gnomAD v4: 10-102832529-TTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832532_102832533del , CM000672.2:g.102832532_102832533del	GRCh38
NC_000010.10:g.104592289_104592290del , CM000672.1:g.104592289_104592290del	GRCh37
NC_000010.9:g.104582279_104582280del	NCBI36
NG_007955.1:g.10003_10004del

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1119_1120del (CYP17A1) MANE Select	ENSP00000358903.3:p.His373GlnfsTer5
ENST00000638190.1:c.816_817del (CYP17A1)	ENSP00000492539.1:p.His272GlnfsTer5
ENST00000638272.1:c.663_664del (CYP17A1)	ENSP00000491508.1:p.His221GlnfsTer5
ENST00000638971.1:c.1032_1033del (CYP17A1)	ENSP00000492313.1:p.His344GlnfsTer5
ENST00000639393.1:c.1119_1120del (CYP17A1)	ENSP00000492651.1:p.His373GlnfsTer5
ENST00000640633.1:n.881_882del (CYP17A1)
ENST00000647664.1:c.*1563_*1564del (WBP1L)	ENSP00000498131.1:n.*1563_*1564del
ENST00000369887.3:c.1119_1120del (CYP17A1)	ENSP00000358903.3:p.His373GlnfsTer5
NM_000102.3:c.1119_1120del (CYP17A1)	NP_000093.1:p.His373GlnfsTer5
NM_000102.4:c.1119_1120del (CYP17A1) MANE Select	NP_000093.1:p.His373GlnfsTer5