Canonical Allele Identifier: CA2668622544

Gene: PIK3CA

Linked Data

• gnomAD v4: 3-179218455-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179218455T>C , CM000665.2:g.179218455T>C	GRCh38
NC_000003.11:g.178936243T>C , CM000665.1:g.178936243T>C	GRCh37
NC_000003.10:g.180418937T>C	NCBI36
NG_012113.2:g.74933T>C , LRG_310:g.74933T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1664+121T>C MANE Select	ENSP00000263967.3:n.1664+121T>C
ENST00000462255.2:n.126+121T>C
ENST00000643187.1:c.1664+121T>C	ENSP00000493507.1:n.1664+121T>C
ENST00000674534.1:n.1539T>C
ENST00000674622.1:c.167+121T>C	ENSP00000502417.1:n.167+121T>C
ENST00000675467.1:n.4471+121T>C
ENST00000675786.1:c.*231+121T>C	ENSP00000502323.1:n.*231+121T>C
ENST00000263967.3:c.1664+121T>C	ENSP00000263967.3:n.1664+121T>C
NM_006218.2:c.1664+121T>C , LRG_310t1:c.1664+121T>C	NP_006209.2:n.1664+121T>C
XM_006713658.2:c.1664+121T>C	XP_006713721.1:n.1664+121T>C
XM_011512894.1:c.1664+121T>C	XP_011511196.1:n.1664+121T>C
NM_006218.3:c.1664+121T>C	NP_006209.2:n.1664+121T>C
XM_006713658.4:c.1664+121T>C	XP_006713721.1:n.1664+121T>C
XM_011512894.2:c.1664+121T>C	XP_011511196.1:n.1664+121T>C
NM_006218.4:c.1664+121T>C MANE Select	NP_006209.2:n.1664+121T>C