Canonical Allele Identifier: CA355285827

Gene: PIK3CA

Linked Data

• dbSNP Id: rs1576949960
• COSMIC: COSM27504 ; COSM1041522
• MyVariant Identifiers: chr3:g.178952077T>G (hg19) ; chr3:g.179234289T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234289T>G , CM000665.2:g.179234289T>G	GRCh38
NC_000003.11:g.178952077T>G , CM000665.1:g.178952077T>G	GRCh37
NC_000003.10:g.180434771T>G	NCBI36
NG_012113.2:g.90767T>G , LRG_310:g.90767T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.3132T>G MANE Select	ENSP00000263967.3:p.Asn1044Lys
ENST00000462255.2:n.2155T>G
ENST00000643187.1:c.*212T>G	ENSP00000493507.1:n.*212T>G
ENST00000674534.1:n.4040T>G
ENST00000674622.1:c.1553T>G	ENSP00000502417.1:n.1553T>G
ENST00000675467.1:n.5939T>G
ENST00000675786.1:c.*1699T>G	ENSP00000502323.1:n.*1699T>G
ENST00000675796.1:n.3027T>G
ENST00000263967.3:c.3132T>G	ENSP00000263967.3:p.Asn1044Lys
NM_006218.2:c.3132T>G , LRG_310t1:c.3132T>G	NP_006209.2:p.Asn1044Lys
XM_006713658.2:c.3132T>G	XP_006713721.1:p.Asn1044Lys
XM_011512894.1:c.3132T>G	XP_011511196.1:p.Asn1044Lys
NM_006218.3:c.3132T>G	NP_006209.2:p.Asn1044Lys
XM_006713658.4:c.3132T>G	XP_006713721.1:p.Asn1044Lys
XM_011512894.2:c.3132T>G	XP_011511196.1:p.Asn1044Lys
NM_006218.4:c.3132T>G MANE Select	NP_006209.2:p.Asn1044Lys