Canonical Allele Identifier: CA891840214

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960906_87960908delinsGCT , CM000672.2:g.87960906_87960908delinsGCT	GRCh38
NC_000010.10:g.89720663_89720665delinsGCT , CM000672.1:g.89720663_89720665delinsGCT	GRCh37
NC_000010.9:g.89710643_89710645delinsGCT	NCBI36
NG_007466.2:g.102468_102470delinsGCT , LRG_311:g.102468_102470delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.907_909delinsGCT	ENSP00000514759.2:p.His303Ala
ENST00000710265.1:c.814_816delinsGCT	ENSP00000518161.1:p.His272Ala
ENST00000472832.3:c.814_816delinsGCT	ENSP00000483066.2:p.His272Ala
ENST00000688158.2:n.1549_1551delinsGCT
ENST00000688922.2:c.*644_*646delinsGCT	ENSP00000508742.2:n.*644_*646delinsGCT
ENST00000700021.1:c.769_771delinsGCT	ENSP00000514757.1:p.His257Ala
ENST00000700022.1:c.*153_*155delinsGCT	ENSP00000514758.1:n.*153_*155delinsGCT
ENST00000700023.1:n.1972_1974delinsGCT
ENST00000700024.1:n.2206_2208delinsGCT
ENST00000700025.1:n.1583_1585delinsGCT
ENST00000700026.1:n.451_453delinsGCT
ENST00000700029.1:c.741_743delinsGCT
ENST00000706954.1:c.814_816delinsGCT	ENSP00000516674.1:p.His272Ala
ENST00000706955.1:c.*849_*851delinsGCT	ENSP00000516675.1:n.*849_*851delinsGCT
ENST00000686459.1:c.*400_*402delinsGCT	ENSP00000508909.1:n.*400_*402delinsGCT
ENST00000688158.1:c.*925_*927delinsGCT	ENSP00000509254.1:n.*925_*927delinsGCT
ENST00000688308.1:c.814_816delinsGCT	ENSP00000508752.1:p.His272Ala
ENST00000688922.1:c.735_737delinsGCT
ENST00000693560.1:c.1333_1335delinsGCT	ENSP00000509861.1:p.His445Ala
ENST00000371953.8:c.814_816delinsGCT MANE Select	ENSP00000361021.3:p.His272Ala
ENST00000371953.7:c.814_816delinsGCT	ENSP00000361021.3:p.His272Ala
ENST00000472832.2:c.241_243delinsGCT	ENSP00000483066.1:p.His81Ala
NM_000314.5:c.814_816delinsGCT	NP_000305.3:p.His272Ala
NM_000314.6:c.814_816delinsGCT	NP_000305.3:p.His272Ala
NM_001304717.2:c.1333_1335delinsGCT	NP_001291646.2:p.His445Ala
NM_001304718.1:c.223_225delinsGCT	NP_001291647.1:p.His75Ala
XM_006717926.2:c.769_771delinsGCT	XP_006717989.1:p.His257Ala
XM_011539981.1:c.814_816delinsGCT	XP_011538283.1:p.His272Ala
XM_011539982.1:c.718_720delinsGCT	XP_011538284.1:p.His240Ala
XR_945791.1:n.1384_1386delinsGCT
NM_000314.7:c.814_816delinsGCT	NP_000305.3:p.His272Ala
NM_001304717.5:c.1333_1335delinsGCT	NP_001291646.4:p.His445Ala
NM_001304718.2:c.223_225delinsGCT	NP_001291647.1:p.His75Ala
NM_000314.8:c.814_816delinsGCT MANE Select	NP_000305.3:p.His272Ala