Canonical Allele Identifier: CA16602917
Gene: PIK3CA HGNC NCBI

Linked Data

ClinVar Variation Id: 376483
dbSNP Id: rs1057519934

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179199158G>C , CM000665.2:g.179199158G>C GRCh38
NC_000003.11:g.178916946G>C , CM000665.1:g.178916946G>C GRCh37
NC_000003.10:g.180399640G>C NCBI36
NG_012113.2:g.55636G>C , LRG_310:g.55636G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.333G>C MANE Select ENSP00000263967.3:p.Lys111Asn
ENST00000643187.1:c.333G>C ENSP00000493507.1:p.Lys111Asn
ENST00000675467.1:n.3140G>C
ENST00000675786.1:c.333G>C ENSP00000502323.1:p.Lys111Asn
ENST00000263967.3:c.333G>C ENSP00000263967.3:p.Lys111Asn
ENST00000468036.1:c.333G>C ENSP00000417479.1:p.Lys111Asn
NM_006218.2:c.333G>C , LRG_310t1:c.333G>C NP_006209.2:p.Lys111Asn
XM_006713658.2:c.333G>C XP_006713721.1:p.Lys111Asn
XM_011512894.1:c.333G>C XP_011511196.1:p.Lys111Asn
NM_006218.3:c.333G>C NP_006209.2:p.Lys111Asn
XM_006713658.4:c.333G>C XP_006713721.1:p.Lys111Asn
XM_011512894.2:c.333G>C XP_011511196.1:p.Lys111Asn
NM_006218.4:c.333G>C MANE Select NP_006209.2:p.Lys111Asn