Canonical Allele Identifier: CA11388440
Gene: PIK3CA HGNC NCBI
COSMIC:
COSN26960250 (not active)
COSN26960251 (not active)
COSN26960252 (not active)
COSN26960253 (not active)
COSN26960254 (not active)
MyVariant.info:
GRCh38 chr3:g.179148620C>T
GRCh37 chr3:g.178866408C>T
gnomAD v2:
3:178866408 C / T
gnomAD v3:
3:179148620 C / T
gnomAD v4:
chr3-179148620-C-T
Joint Max Group AF 0.24318555 (NFE)
Genomes Max Group AF 0.24312411 (NFE)
Exomes Max Group AF 0.21269427 (NFE)
dbSNP:
2699887
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179148620C>T , CM000665.2:g.179148620C>T GRCh38
NC_000003.11:g.178866408C>T , CM000665.1:g.178866408C>T GRCh37
NC_000003.10:g.180349102C>T NCBI36
NG_012113.2:g.5098C>T , LRG_310:g.5098C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.-77+17C>T MANE Select ENSP00000263967.3:n.-77+17C>T
ENST00000643187.1:c.-77+17C>T ENSP00000493507.1:n.-77+17C>T
ENST00000263967.3:c.-77+17C>T ENSP00000263967.3:n.-77+17C>T
ENST00000477735.1:c.-77+401C>T ENSP00000418145.1:n.-77+401C>T
NM_006218.2:c.-77+17C>T , LRG_310t1:c.-77+17C>T NP_006209.2:n.-77+17C>T
XM_006713658.2:c.-77+401C>T XP_006713721.1:n.-77+401C>T
NM_006218.3:c.-77+17C>T NP_006209.2:n.-77+17C>T
XM_006713658.4:c.-77+401C>T XP_006713721.1:n.-77+401C>T
NM_006218.4:c.-77+17C>T MANE Select NP_006209.2:n.-77+17C>T
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