Canonical Allele Identifier: CA2573136780

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 1382307
• ClinVar RCV Id: RCV001897575
• dbSNP Id: rs2108392531

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179203561_179203563del , CM000665.2:g.179203561_179203563del	GRCh38
NC_000003.11:g.178921349_178921351del , CM000665.1:g.178921349_178921351del	GRCh37
NC_000003.10:g.180404043_180404045del	NCBI36
NG_012113.2:g.60039_60041del , LRG_310:g.60039_60041del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.831_833del MANE Select	ENSP00000263967.3:p.Ile277del
ENST00000643187.1:c.831_833del	ENSP00000493507.1:p.Ile277del
ENST00000674534.1:n.585_587del
ENST00000675467.1:n.3638_3640del
ENST00000675786.1:c.831_833del	ENSP00000502323.1:p.Ile277del
ENST00000263967.3:c.831_833del	ENSP00000263967.3:p.Ile277del
NM_006218.2:c.831_833del , LRG_310t1:c.831_833del	NP_006209.2:p.Ile277del
XM_006713658.2:c.831_833del	XP_006713721.1:p.Ile277del
XM_011512894.1:c.831_833del	XP_011511196.1:p.Ile277del
NM_006218.3:c.831_833del	NP_006209.2:p.Ile277del
XM_006713658.4:c.831_833del	XP_006713721.1:p.Ile277del
XM_011512894.2:c.831_833del	XP_011511196.1:p.Ile277del
NM_006218.4:c.831_833del MANE Select	NP_006209.2:p.Ile277del