Canonical Allele Identifier: CA2832598127

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234393T>G , CM000665.2:g.179234393T>G	GRCh38
NC_000003.11:g.178952181T>G , CM000665.1:g.178952181T>G	GRCh37
NC_000003.10:g.180434875T>G	NCBI36
NG_012113.2:g.90871T>G , LRG_310:g.90871T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.*29T>G MANE Select	ENSP00000263967.3:n.*29T>G
ENST00000462255.2:n.2259T>G
ENST00000643187.1:c.*316T>G	ENSP00000493507.1:n.*316T>G
ENST00000674534.1:n.4144T>G
ENST00000674622.1:c.1657T>G	ENSP00000502417.1:n.1657T>G
ENST00000675467.1:n.6043T>G
ENST00000675786.1:c.*1803T>G	ENSP00000502323.1:n.*1803T>G
ENST00000675796.1:n.3131T>G
ENST00000263967.3:c.*29T>G	ENSP00000263967.3:n.*29T>G
NM_006218.2:c.*29T>G , LRG_310t1:c.*29T>G	NP_006209.2:n.*29T>G
XM_006713658.2:c.*29T>G	XP_006713721.1:n.*29T>G
XM_011512894.1:c.*29T>G	XP_011511196.1:n.*29T>G
NM_006218.3:c.*29T>G	NP_006209.2:n.*29T>G
XM_006713658.4:c.*29T>G	XP_006713721.1:n.*29T>G
XM_011512894.2:c.*29T>G	XP_011511196.1:n.*29T>G
NM_006218.4:c.*29T>G MANE Select	NP_006209.2:n.*29T>G