Canonical Allele Identifier: CA355278641
Community Standard Title: NM_006218.4(PIK3CA):c.813+2T>C
Gene: PIK3CA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179201542T>C , CM000665.2:g.179201542T>C GRCh38
NC_000003.11:g.178919330T>C , CM000665.1:g.178919330T>C GRCh37
NC_000003.10:g.180402024T>C NCBI36
NG_012113.2:g.58020T>C , LRG_310:g.58020T>C

Transcript Alleles

HGVS Amino-acid Change
NM_006218.4:c.813+2T>C MANE Select NP_006209.2:n.813+2T>C
ENST00000263967.4:c.813+2T>C MANE Select ENSP00000263967.3:n.813+2T>C
NM_006218.2:c.813+2T>C , LRG_310t1:c.813+2T>C NP_006209.2:n.813+2T>C
NM_006218.3:c.813+2T>C NP_006209.2:n.813+2T>C
ENST00000263967.3:c.813+2T>C ENSP00000263967.3:n.813+2T>C
ENST00000643187.1:c.813+2T>C ENSP00000493507.1:n.813+2T>C
ENST00000675467.1:n.3620+2T>C
ENST00000675786.1:c.813+2T>C ENSP00000502323.1:n.813+2T>C
XM_006713658.2:c.813+2T>C XP_006713721.1:n.813+2T>C
XM_006713658.4:c.813+2T>C XP_006713721.1:n.813+2T>C
XM_011512894.1:c.813+2T>C XP_011511196.1:n.813+2T>C
XM_011512894.2:c.813+2T>C XP_011511196.1:n.813+2T>C