Canonical Allele Identifier: CA2704642182
Gene: PIK3CA HGNC NCBI

Linked Data

dbSNP Id: rs2108408921

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179218477G>C , CM000665.2:g.179218477G>C GRCh38
NC_000003.11:g.178936265G>C , CM000665.1:g.178936265G>C GRCh37
NC_000003.10:g.180418959G>C NCBI36
NG_012113.2:g.74955G>C , LRG_310:g.74955G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.1664+143G>C MANE Select ENSP00000263967.3:n.1664+143G>C
ENST00000462255.2:n.126+143G>C
ENST00000643187.1:c.1664+143G>C ENSP00000493507.1:n.1664+143G>C
ENST00000674534.1:n.1561G>C
ENST00000674622.1:c.167+143G>C ENSP00000502417.1:n.167+143G>C
ENST00000675467.1:n.4471+143G>C
ENST00000675786.1:c.*231+143G>C ENSP00000502323.1:n.*231+143G>C
ENST00000263967.3:c.1664+143G>C ENSP00000263967.3:n.1664+143G>C
NM_006218.2:c.1664+143G>C , LRG_310t1:c.1664+143G>C NP_006209.2:n.1664+143G>C
XM_006713658.2:c.1664+143G>C XP_006713721.1:n.1664+143G>C
XM_011512894.1:c.1664+143G>C XP_011511196.1:n.1664+143G>C
NM_006218.3:c.1664+143G>C NP_006209.2:n.1664+143G>C
XM_006713658.4:c.1664+143G>C XP_006713721.1:n.1664+143G>C
XM_011512894.2:c.1664+143G>C XP_011511196.1:n.1664+143G>C
NM_006218.4:c.1664+143G>C MANE Select NP_006209.2:n.1664+143G>C