Canonical Allele Identifier: CA2579927110

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925557_87925558delinsCA , CM000672.2:g.87925557_87925558delinsCA	GRCh38
NC_000010.10:g.89685314_89685315delinsCA , CM000672.1:g.89685314_89685315delinsCA	GRCh37
NC_000010.9:g.89675294_89675295delinsCA	NCBI36
NG_007466.2:g.67119_67120delinsCA , LRG_311:g.67119_67120delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.209_209+1delinsCA
ENST00000710265.1:c.209_209+1delinsCA
ENST00000472832.3:c.209_209+1delinsCA
ENST00000688158.2:n.944_944+1delinsCA
ENST00000688922.2:c.209_209+1delinsCA
ENST00000700021.1:c.165-5489_165-5488delinsCA	ENSP00000514757.1:n.165-5489_165-5488delinsCA
ENST00000700022.1:c.209_209+1delinsCA
ENST00000700029.1:c.43_43+1delinsCA
ENST00000706954.1:c.209_209+1delinsCA
ENST00000706955.1:c.*244_*244+1delinsCA
ENST00000686459.1:c.209_209+1delinsCA
ENST00000688158.1:c.*320_*320+1delinsCA
ENST00000688308.1:c.209_209+1delinsCA
ENST00000688922.1:c.78_78+1delinsCA
ENST00000693560.1:c.728_728+1delinsCA
ENST00000371953.8:c.209_209+1delinsCA
ENST00000371953.7:c.209_209+1delinsCA
ENST00000498703.1:n.35_35+1delinsCA
ENST00000610634.1:c.107_107+1delinsCA
NM_000314.5:c.209_209+1delinsCA
NM_000314.6:c.209_209+1delinsCA
NM_001304717.2:c.728_728+1delinsCA
NM_001304718.1:c.-541-5489_-541-5488delinsCA	NP_001291647.1:n.-541-5489_-541-5488delinsCA
XM_006717926.2:c.165-5489_165-5488delinsCA	XP_006717989.1:n.165-5489_165-5488delinsCA
XM_011539981.1:c.209_209+1delinsCA
XM_011539982.1:c.113_113+1delinsCA
XR_945789.1:n.921_921+1delinsCA
XR_945790.1:n.921_921+1delinsCA
XR_945791.1:n.921_921+1delinsCA
NM_000314.7:c.209_209+1delinsCA
NM_001304717.5:c.728_728+1delinsCA
NM_001304718.2:c.-541-5489_-541-5488delinsCA	NP_001291647.1:n.-541-5489_-541-5488delinsCA
NM_000314.8:c.209_209+1delinsCA