Canonical Allele Identifier: CA2668622536

Gene: PIK3CA

Linked Data

• gnomAD v4: 3-179218439-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179218442del , CM000665.2:g.179218442del	GRCh38
NC_000003.11:g.178936230del , CM000665.1:g.178936230del	GRCh37
NC_000003.10:g.180418924del	NCBI36
NG_012113.2:g.74920del , LRG_310:g.74920del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1664+108del MANE Select	ENSP00000263967.3:n.1664+108del
ENST00000462255.2:n.126+108del
ENST00000643187.1:c.1664+108del	ENSP00000493507.1:n.1664+108del
ENST00000674534.1:n.1526del
ENST00000674622.1:c.167+108del	ENSP00000502417.1:n.167+108del
ENST00000675467.1:n.4471+108del
ENST00000675786.1:c.*231+108del	ENSP00000502323.1:n.*231+108del
ENST00000263967.3:c.1664+108del	ENSP00000263967.3:n.1664+108del
NM_006218.2:c.1664+108del , LRG_310t1:c.1664+108del	NP_006209.2:n.1664+108del
XM_006713658.2:c.1664+108del	XP_006713721.1:n.1664+108del
XM_011512894.1:c.1664+108del	XP_011511196.1:n.1664+108del
NM_006218.3:c.1664+108del	NP_006209.2:n.1664+108del
XM_006713658.4:c.1664+108del	XP_006713721.1:n.1664+108del
XM_011512894.2:c.1664+108del	XP_011511196.1:n.1664+108del
NM_006218.4:c.1664+108del MANE Select	NP_006209.2:n.1664+108del