Canonical Allele Identifier: CA2668599353

Gene: PIK3CA

Linked Data

• gnomAD v4: 3-179234261-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234264dup , CM000665.2:g.179234264dup	GRCh38
NC_000003.11:g.178952052dup , CM000665.1:g.178952052dup	GRCh37
NC_000003.10:g.180434746dup	NCBI36
NG_012113.2:g.90742dup , LRG_310:g.90742dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.3107dup MANE Select	ENSP00000263967.3:p.Leu1036PhefsTer10
ENST00000462255.2:n.2130dup
ENST00000643187.1:c.*187dup	ENSP00000493507.1:n.*187dup
ENST00000674534.1:n.4015dup
ENST00000674622.1:c.1528dup	ENSP00000502417.1:n.1528dup
ENST00000675467.1:n.5914dup
ENST00000675786.1:c.*1674dup	ENSP00000502323.1:n.*1674dup
ENST00000675796.1:n.3002dup
ENST00000263967.3:c.3107dup	ENSP00000263967.3:p.Leu1036PhefsTer10
NM_006218.2:c.3107dup , LRG_310t1:c.3107dup	NP_006209.2:p.Leu1036PhefsTer10
XM_006713658.2:c.3107dup	XP_006713721.1:p.Leu1036PhefsTer10
XM_011512894.1:c.3107dup	XP_011511196.1:p.Leu1036PhefsTer10
NM_006218.3:c.3107dup	NP_006209.2:p.Leu1036PhefsTer10
XM_006713658.4:c.3107dup	XP_006713721.1:p.Leu1036PhefsTer10
XM_011512894.2:c.3107dup	XP_011511196.1:p.Leu1036PhefsTer10
NM_006218.4:c.3107dup MANE Select	NP_006209.2:p.Leu1036PhefsTer10