Canonical Allele Identifier: CA355279223

Gene: PIK3CA

Linked Data

• dbSNP Id: rs2108423957
• MyVariant Identifiers: chr3:g.178947796G>T (hg19) ; chr3:g.179230008G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179230008G>T , CM000665.2:g.179230008G>T	GRCh38
NC_000003.11:g.178947796G>T , CM000665.1:g.178947796G>T	GRCh37
NC_000003.10:g.180430490G>T	NCBI36
NG_012113.2:g.86486G>T , LRG_310:g.86486G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.2671G>T MANE Select	ENSP00000263967.3:p.Asp891Tyr
ENST00000462255.2:n.1694G>T
ENST00000643187.1:c.2671G>T	ENSP00000493507.1:p.Asp891Tyr
ENST00000674534.1:n.3579G>T
ENST00000674622.1:c.1092G>T	ENSP00000502417.1:n.1092G>T
ENST00000675467.1:n.5478G>T
ENST00000675786.1:c.*1238G>T	ENSP00000502323.1:n.*1238G>T
ENST00000675796.1:n.2566G>T
ENST00000263967.3:c.2671G>T	ENSP00000263967.3:p.Asp891Tyr
NM_006218.2:c.2671G>T , LRG_310t1:c.2671G>T	NP_006209.2:p.Asp891Tyr
XM_006713658.2:c.2671G>T	XP_006713721.1:p.Asp891Tyr
XM_011512894.1:c.2671G>T	XP_011511196.1:p.Asp891Tyr
NM_006218.3:c.2671G>T	NP_006209.2:p.Asp891Tyr
XM_006713658.4:c.2671G>T	XP_006713721.1:p.Asp891Tyr
XM_011512894.2:c.2671G>T	XP_011511196.1:p.Asp891Tyr
NM_006218.4:c.2671G>T MANE Select	NP_006209.2:p.Asp891Tyr