Canonical Allele Identifier: CA2579927109

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925556_87925558delinsAAA , CM000672.2:g.87925556_87925558delinsAAA	GRCh38
NC_000010.10:g.89685313_89685315delinsAAA , CM000672.1:g.89685313_89685315delinsAAA	GRCh37
NC_000010.9:g.89675293_89675295delinsAAA	NCBI36
NG_007466.2:g.67118_67120delinsAAA , LRG_311:g.67118_67120delinsAAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.208_209+1delinsAAA
ENST00000710265.1:c.208_209+1delinsAAA
ENST00000472832.3:c.208_209+1delinsAAA
ENST00000688158.2:n.943_944+1delinsAAA
ENST00000688922.2:c.208_209+1delinsAAA
ENST00000700021.1:c.165-5490_165-5488delinsAAA	ENSP00000514757.1:n.165-5490_165-5488deli...
ENST00000700022.1:c.208_209+1delinsAAA
ENST00000700029.1:c.42_43+1delinsAAA
ENST00000706954.1:c.208_209+1delinsAAA
ENST00000706955.1:c.*243_*244+1delinsAAA
ENST00000686459.1:c.208_209+1delinsAAA
ENST00000688158.1:c.*319_*320+1delinsAAA
ENST00000688308.1:c.208_209+1delinsAAA
ENST00000688922.1:c.77_78+1delinsAAA
ENST00000693560.1:c.727_728+1delinsAAA
ENST00000371953.8:c.208_209+1delinsAAA
ENST00000371953.7:c.208_209+1delinsAAA
ENST00000498703.1:n.34_35+1delinsAAA
ENST00000610634.1:c.106_107+1delinsAAA
NM_000314.5:c.208_209+1delinsAAA
NM_000314.6:c.208_209+1delinsAAA
NM_001304717.2:c.727_728+1delinsAAA
NM_001304718.1:c.-541-5490_-541-5488delinsAAA	NP_001291647.1:n.-541-5490_-541-5488delin...
XM_006717926.2:c.165-5490_165-5488delinsAAA	XP_006717989.1:n.165-5490_165-5488delinsA...
XM_011539981.1:c.208_209+1delinsAAA
XM_011539982.1:c.112_113+1delinsAAA
XR_945789.1:n.920_921+1delinsAAA
XR_945790.1:n.920_921+1delinsAAA
XR_945791.1:n.920_921+1delinsAAA
NM_000314.7:c.208_209+1delinsAAA
NM_001304717.5:c.727_728+1delinsAAA
NM_001304718.2:c.-541-5490_-541-5488delinsAAA	NP_001291647.1:n.-541-5490_-541-5488delin...
NM_000314.8:c.208_209+1delinsAAA