Canonical Allele Identifier: CA2668622322
Gene: PIK3CA HGNC NCBI

Linked Data

dbSNP Id: rs2108407880

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179218203T>C , CM000665.2:g.179218203T>C GRCh38
NC_000003.11:g.178935991T>C , CM000665.1:g.178935991T>C GRCh37
NC_000003.10:g.180418685T>C NCBI36
NG_012113.2:g.74681T>C , LRG_310:g.74681T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263967.4:c.1540-7T>C MANE Select ENSP00000263967.3:n.1540-7T>C
ENST00000643187.1:c.1540-7T>C ENSP00000493507.1:n.1540-7T>C
ENST00000674534.1:n.1294-7T>C
ENST00000674622.1:c.43-7T>C ENSP00000502417.1:n.43-7T>C
ENST00000675467.1:n.4347-7T>C
ENST00000675786.1:c.*107-7T>C ENSP00000502323.1:n.*107-7T>C
ENST00000263967.3:c.1540-7T>C ENSP00000263967.3:n.1540-7T>C
NM_006218.2:c.1540-7T>C , LRG_310t1:c.1540-7T>C NP_006209.2:n.1540-7T>C
XM_006713658.2:c.1540-7T>C XP_006713721.1:n.1540-7T>C
XM_011512894.1:c.1540-7T>C XP_011511196.1:n.1540-7T>C
NM_006218.3:c.1540-7T>C NP_006209.2:n.1540-7T>C
XM_006713658.4:c.1540-7T>C XP_006713721.1:n.1540-7T>C
XM_011512894.2:c.1540-7T>C XP_011511196.1:n.1540-7T>C
NM_006218.4:c.1540-7T>C MANE Select NP_006209.2:n.1540-7T>C