Canonical Allele Identifier: CA355285780

Gene: PIK3CA

Linked Data

• dbSNP Id: rs2108429791
• COSMIC: COSM86043
• MyVariant Identifiers: chr3:g.178952063A>T (hg19) ; chr3:g.179234275A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234275A>T , CM000665.2:g.179234275A>T	GRCh38
NC_000003.11:g.178952063A>T , CM000665.1:g.178952063A>T	GRCh37
NC_000003.10:g.180434757A>T	NCBI36
NG_012113.2:g.90753A>T , LRG_310:g.90753A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.3118A>T MANE Select	ENSP00000263967.3:p.Met1040Leu
ENST00000462255.2:n.2141A>T
ENST00000643187.1:c.*198A>T	ENSP00000493507.1:n.*198A>T
ENST00000674534.1:n.4026A>T
ENST00000674622.1:c.1539A>T	ENSP00000502417.1:n.1539A>T
ENST00000675467.1:n.5925A>T
ENST00000675786.1:c.*1685A>T	ENSP00000502323.1:n.*1685A>T
ENST00000675796.1:n.3013A>T
ENST00000263967.3:c.3118A>T	ENSP00000263967.3:p.Met1040Leu
NM_006218.2:c.3118A>T , LRG_310t1:c.3118A>T	NP_006209.2:p.Met1040Leu
XM_006713658.2:c.3118A>T	XP_006713721.1:p.Met1040Leu
XM_011512894.1:c.3118A>T	XP_011511196.1:p.Met1040Leu
NM_006218.3:c.3118A>T	NP_006209.2:p.Met1040Leu
XM_006713658.4:c.3118A>T	XP_006713721.1:p.Met1040Leu
XM_011512894.2:c.3118A>T	XP_011511196.1:p.Met1040Leu
NM_006218.4:c.3118A>T MANE Select	NP_006209.2:p.Met1040Leu