Canonical Allele Identifier: CA355262620
Community Standard Title: NM_006218.4(PIK3CA):c.1480G>C (p.Glu494Gln)
Gene: PIK3CA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179210506G>C , CM000665.2:g.179210506G>C GRCh38
NC_000003.11:g.178928294G>C , CM000665.1:g.178928294G>C GRCh37
NC_000003.10:g.180410988G>C NCBI36
NG_012113.2:g.66984G>C , LRG_310:g.66984G>C

Transcript Alleles

HGVS Amino-acid Change
NM_006218.4:c.1480G>C MANE Select NP_006209.2:p.Glu494Gln
ENST00000263967.4:c.1480G>C MANE Select ENSP00000263967.3:p.Glu494Gln
NM_006218.2:c.1480G>C , LRG_310t1:c.1480G>C NP_006209.2:p.Glu494Gln
NM_006218.3:c.1480G>C NP_006209.2:p.Glu494Gln
ENST00000263967.3:c.1480G>C ENSP00000263967.3:p.Glu494Gln
ENST00000643187.1:c.1480G>C ENSP00000493507.1:p.Glu494Gln
ENST00000674534.1:n.1234G>C
ENST00000675467.1:n.4287G>C
ENST00000675786.1:c.*47G>C ENSP00000502323.1:n.*47G>C
XM_006713658.2:c.1480G>C XP_006713721.1:p.Glu494Gln
XM_006713658.4:c.1480G>C XP_006713721.1:p.Glu494Gln
XM_011512894.1:c.1480G>C XP_011511196.1:p.Glu494Gln
XM_011512894.2:c.1480G>C XP_011511196.1:p.Glu494Gln