Canonical Allele Identifier: CA355279202

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 1997328
• ClinVar RCV Id: RCV002791713
• MyVariant Identifiers: chr3:g.178947793T>G (hg19) ; chr3:g.179230005T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179230005T>G , CM000665.2:g.179230005T>G	GRCh38
NC_000003.11:g.178947793T>G , CM000665.1:g.178947793T>G	GRCh37
NC_000003.10:g.180430487T>G	NCBI36
NG_012113.2:g.86483T>G , LRG_310:g.86483T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.2668T>G MANE Select	ENSP00000263967.3:p.Tyr890Asp
ENST00000462255.2:n.1691T>G
ENST00000643187.1:c.2668T>G	ENSP00000493507.1:p.Tyr890Asp
ENST00000674534.1:n.3576T>G
ENST00000674622.1:c.1089T>G	ENSP00000502417.1:n.1089T>G
ENST00000675467.1:n.5475T>G
ENST00000675786.1:c.*1235T>G	ENSP00000502323.1:n.*1235T>G
ENST00000675796.1:n.2563T>G
ENST00000263967.3:c.2668T>G	ENSP00000263967.3:p.Tyr890Asp
NM_006218.2:c.2668T>G , LRG_310t1:c.2668T>G	NP_006209.2:p.Tyr890Asp
XM_006713658.2:c.2668T>G	XP_006713721.1:p.Tyr890Asp
XM_011512894.1:c.2668T>G	XP_011511196.1:p.Tyr890Asp
NM_006218.3:c.2668T>G	NP_006209.2:p.Tyr890Asp
XM_006713658.4:c.2668T>G	XP_006713721.1:p.Tyr890Asp
XM_011512894.2:c.2668T>G	XP_011511196.1:p.Tyr890Asp
NM_006218.4:c.2668T>G MANE Select	NP_006209.2:p.Tyr890Asp