Canonical Allele Identifier: CA355266894
Community Standard Title: NM_006218.4(PIK3CA):c.1873G>A (p.Asp625Asn)
Gene: PIK3CA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179219697G>A , CM000665.2:g.179219697G>A GRCh38
NC_000003.11:g.178937485G>A , CM000665.1:g.178937485G>A GRCh37
NC_000003.10:g.180420179G>A NCBI36
NG_012113.2:g.76175G>A , LRG_310:g.76175G>A

Transcript Alleles

HGVS Amino-acid Change
NM_006218.4:c.1873G>A MANE Select NP_006209.2:p.Asp625Asn
ENST00000263967.4:c.1873G>A MANE Select ENSP00000263967.3:p.Asp625Asn
NM_006218.2:c.1873G>A , LRG_310t1:c.1873G>A NP_006209.2:p.Asp625Asn
NM_006218.3:c.1873G>A NP_006209.2:p.Asp625Asn
ENST00000263967.3:c.1873G>A ENSP00000263967.3:p.Asp625Asn
ENST00000462255.1:n.147G>A
ENST00000462255.2:n.335G>A
ENST00000643187.1:c.1873G>A ENSP00000493507.1:p.Asp625Asn
ENST00000674534.1:n.2781G>A
ENST00000674622.1:c.294G>A ENSP00000502417.1:n.294G>A
ENST00000675467.1:n.4680G>A
ENST00000675786.1:c.*440G>A ENSP00000502323.1:n.*440G>A
XM_006713658.2:c.1873G>A XP_006713721.1:p.Asp625Asn
XM_006713658.4:c.1873G>A XP_006713721.1:p.Asp625Asn
XM_011512894.1:c.1873G>A XP_011511196.1:p.Asp625Asn
XM_011512894.2:c.1873G>A XP_011511196.1:p.Asp625Asn