Canonical Allele Identifier: CA355265856
Gene: PIK3CA HGNC NCBI

Linked Data

dbSNP Id: rs1174763085

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179219588A>T , CM000665.2:g.179219588A>T GRCh38
NC_000003.11:g.178937376A>T , CM000665.1:g.178937376A>T GRCh37
NC_000003.10:g.180420070A>T NCBI36
NG_012113.2:g.76066A>T , LRG_310:g.76066A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.1764A>T MANE Select ENSP00000263967.3:p.Lys588Asn
ENST00000462255.2:n.226A>T
ENST00000643187.1:c.1764A>T ENSP00000493507.1:p.Lys588Asn
ENST00000674534.1:n.2672A>T
ENST00000674622.1:c.185A>T ENSP00000502417.1:n.185A>T
ENST00000675467.1:n.4571A>T
ENST00000675786.1:c.*331A>T ENSP00000502323.1:n.*331A>T
ENST00000263967.3:c.1764A>T ENSP00000263967.3:p.Lys588Asn
ENST00000462255.1:n.38A>T
NM_006218.2:c.1764A>T , LRG_310t1:c.1764A>T NP_006209.2:p.Lys588Asn
XM_006713658.2:c.1764A>T XP_006713721.1:p.Lys588Asn
XM_011512894.1:c.1764A>T XP_011511196.1:p.Lys588Asn
NM_006218.3:c.1764A>T NP_006209.2:p.Lys588Asn
XM_006713658.4:c.1764A>T XP_006713721.1:p.Lys588Asn
XM_011512894.2:c.1764A>T XP_011511196.1:p.Lys588Asn
NM_006218.4:c.1764A>T MANE Select NP_006209.2:p.Lys588Asn