Canonical Allele Identifier: CA2610724239

Gene: CYP17A1

Linked Data

• gnomAD v4: 10-102834807-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102834809del , CM000672.2:g.102834809del	GRCh38
NC_000010.10:g.104594566del , CM000672.1:g.104594566del	GRCh37
NC_000010.9:g.104584556del	NCBI36
NG_007955.1:g.7726del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.643del MANE Select	ENSP00000358903.3:p.Val215TrpfsTer3
ENST00000638190.1:c.643del	ENSP00000492539.1:p.Val215TrpfsTer3
ENST00000638272.1:c.298-1600del	ENSP00000491508.1:n.298-1600del
ENST00000638971.1:c.643del	ENSP00000492313.1:p.Val215TrpfsTer3
ENST00000639393.1:c.643del	ENSP00000492651.1:p.Val215TrpfsTer3
ENST00000640633.1:n.405del
ENST00000369887.3:c.643del	ENSP00000358903.3:p.Val215TrpfsTer3
ENST00000489268.1:n.897del
NM_000102.3:c.643del	NP_000093.1:p.Val215TrpfsTer3
NM_000102.4:c.643del MANE Select	NP_000093.1:p.Val215TrpfsTer3