Canonical Allele Identifier: CA16602928
Gene: PIK3CA HGNC NCBI

Linked Data

ClinVar Variation Id: 376496
dbSNP Id: rs749415085

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179198937C>G , CM000665.2:g.179198937C>G GRCh38
NC_000003.11:g.178916725C>G , CM000665.1:g.178916725C>G GRCh37
NC_000003.10:g.180399419C>G NCBI36
NG_012113.2:g.55415C>G , LRG_310:g.55415C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263967.4:c.112C>G MANE Select ENSP00000263967.3:p.Arg38Gly
ENST00000643187.1:c.112C>G ENSP00000493507.1:p.Arg38Gly
ENST00000675467.1:n.2919C>G
ENST00000675786.1:c.112C>G ENSP00000502323.1:p.Arg38Gly
ENST00000263967.3:c.112C>G ENSP00000263967.3:p.Arg38Gly
ENST00000468036.1:c.112C>G ENSP00000417479.1:p.Arg38Gly
NM_006218.2:c.112C>G , LRG_310t1:c.112C>G NP_006209.2:p.Arg38Gly
XM_006713658.2:c.112C>G XP_006713721.1:p.Arg38Gly
XM_011512894.1:c.112C>G XP_011511196.1:p.Arg38Gly
NM_006218.3:c.112C>G NP_006209.2:p.Arg38Gly
XM_006713658.4:c.112C>G XP_006713721.1:p.Arg38Gly
XM_011512894.2:c.112C>G XP_011511196.1:p.Arg38Gly
NM_006218.4:c.112C>G MANE Select NP_006209.2:p.Arg38Gly