Canonical Allele Identifier: CA891840208

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960906_87960908delinsAGA , CM000672.2:g.87960906_87960908delinsAGA	GRCh38
NC_000010.10:g.89720663_89720665delinsAGA , CM000672.1:g.89720663_89720665delinsAGA	GRCh37
NC_000010.9:g.89710643_89710645delinsAGA	NCBI36
NG_007466.2:g.102468_102470delinsAGA , LRG_311:g.102468_102470delinsAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.907_909delinsAGA	ENSP00000514759.2:p.His303Arg
ENST00000710265.1:c.814_816delinsAGA	ENSP00000518161.1:p.His272Arg
ENST00000472832.3:c.814_816delinsAGA	ENSP00000483066.2:p.His272Arg
ENST00000688158.2:n.1549_1551delinsAGA
ENST00000688922.2:c.*644_*646delinsAGA	ENSP00000508742.2:n.*644_*646delinsAGA
ENST00000700021.1:c.769_771delinsAGA	ENSP00000514757.1:p.His257Arg
ENST00000700022.1:c.*153_*155delinsAGA	ENSP00000514758.1:n.*153_*155delinsAGA
ENST00000700023.1:n.1972_1974delinsAGA
ENST00000700024.1:n.2206_2208delinsAGA
ENST00000700025.1:n.1583_1585delinsAGA
ENST00000700026.1:n.451_453delinsAGA
ENST00000700029.1:c.741_743delinsAGA
ENST00000706954.1:c.814_816delinsAGA	ENSP00000516674.1:p.His272Arg
ENST00000706955.1:c.*849_*851delinsAGA	ENSP00000516675.1:n.*849_*851delinsAGA
ENST00000686459.1:c.*400_*402delinsAGA	ENSP00000508909.1:n.*400_*402delinsAGA
ENST00000688158.1:c.*925_*927delinsAGA	ENSP00000509254.1:n.*925_*927delinsAGA
ENST00000688308.1:c.814_816delinsAGA	ENSP00000508752.1:p.His272Arg
ENST00000688922.1:c.735_737delinsAGA
ENST00000693560.1:c.1333_1335delinsAGA	ENSP00000509861.1:p.His445Arg
ENST00000371953.8:c.814_816delinsAGA MANE Select	ENSP00000361021.3:p.His272Arg
ENST00000371953.7:c.814_816delinsAGA	ENSP00000361021.3:p.His272Arg
ENST00000472832.2:c.241_243delinsAGA	ENSP00000483066.1:p.His81Arg
NM_000314.5:c.814_816delinsAGA	NP_000305.3:p.His272Arg
NM_000314.6:c.814_816delinsAGA	NP_000305.3:p.His272Arg
NM_001304717.2:c.1333_1335delinsAGA	NP_001291646.2:p.His445Arg
NM_001304718.1:c.223_225delinsAGA	NP_001291647.1:p.His75Arg
XM_006717926.2:c.769_771delinsAGA	XP_006717989.1:p.His257Arg
XM_011539981.1:c.814_816delinsAGA	XP_011538283.1:p.His272Arg
XM_011539982.1:c.718_720delinsAGA	XP_011538284.1:p.His240Arg
XR_945791.1:n.1384_1386delinsAGA
NM_000314.7:c.814_816delinsAGA	NP_000305.3:p.His272Arg
NM_001304717.5:c.1333_1335delinsAGA	NP_001291646.4:p.His445Arg
NM_001304718.2:c.223_225delinsAGA	NP_001291647.1:p.His75Arg
NM_000314.8:c.814_816delinsAGA MANE Select	NP_000305.3:p.His272Arg