Canonical Allele Identifier: CA2704641911
Gene: PIK3CA HGNC NCBI

Linked Data

dbSNP Id: rs2108408527

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179218344_179218345insGTCTGTTACTCTGT , CM000665.2:g.179218344_179218345insGTCTGTTACTCTGT GRCh38
NC_000003.11:g.178936132_178936133insGTCTGTTACTCTGT , CM000665.1:g.178936132_178936133insGTCTGTTACTCTGT GRCh37
NC_000003.10:g.180418826_180418827insGTCTGTTACTCTGT NCBI36
NG_012113.2:g.74822_74823insGTCTGTTACTCTGT , LRG_310:g.74822_74823insGTCTGTTACTCTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.1664+10_1664+11insGTCTGTTACTCTGT MANE Select ENSP00000263967.3:n.1664+10_1664+11insGTCTGTTACTCTGT
ENST00000462255.2:n.126+10_126+11insGTCTGTTACTCTGT
ENST00000643187.1:c.1664+10_1664+11insGTCTGTTACTCTGT ENSP00000493507.1:n.1664+10_1664+11insGTCTGTTACTCTGT
ENST00000674534.1:n.1428_1429insGTCTGTTACTCTGT
ENST00000674622.1:c.167+10_167+11insGTCTGTTACTCTGT ENSP00000502417.1:n.167+10_167+11insGTCTGTTACTCTGT
ENST00000675467.1:n.4471+10_4471+11insGTCTGTTACTCTGT
ENST00000675786.1:c.*231+10_*231+11insGTCTGTTACTCTGT ENSP00000502323.1:n.*231+10_*231+11insGTCTGTTACTCTGT
ENST00000263967.3:c.1664+10_1664+11insGTCTGTTACTCTGT ENSP00000263967.3:n.1664+10_1664+11insGTCTGTTACTCTGT
NM_006218.2:c.1664+10_1664+11insGTCTGTTACTCTGT , LRG_310t1:c.1664+10_1664+11insGTCTGTTACTCTGT NP_006209.2:n.1664+10_1664+11insGTCTGTTACTCTGT
XM_006713658.2:c.1664+10_1664+11insGTCTGTTACTCTGT XP_006713721.1:n.1664+10_1664+11insGTCTGTTACTCTGT
XM_011512894.1:c.1664+10_1664+11insGTCTGTTACTCTGT XP_011511196.1:n.1664+10_1664+11insGTCTGTTACTCTGT
NM_006218.3:c.1664+10_1664+11insGTCTGTTACTCTGT NP_006209.2:n.1664+10_1664+11insGTCTGTTACTCTGT
XM_006713658.4:c.1664+10_1664+11insGTCTGTTACTCTGT XP_006713721.1:n.1664+10_1664+11insGTCTGTTACTCTGT
XM_011512894.2:c.1664+10_1664+11insGTCTGTTACTCTGT XP_011511196.1:n.1664+10_1664+11insGTCTGTTACTCTGT
NM_006218.4:c.1664+10_1664+11insGTCTGTTACTCTGT MANE Select NP_006209.2:n.1664+10_1664+11insGTCTGTTACTCTGT