Canonical Allele Identifier: CA891840990

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960900_87960901delinsGG , CM000672.2:g.87960900_87960901delinsGG	GRCh38
NC_000010.10:g.89720657_89720658delinsGG , CM000672.1:g.89720657_89720658delinsGG	GRCh37
NC_000010.9:g.89710637_89710638delinsGG	NCBI36
NG_007466.2:g.102462_102463delinsGG , LRG_311:g.102462_102463delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.901_902delinsGG	ENSP00000514759.2:p.Met301Gly
ENST00000710265.1:c.808_809delinsGG	ENSP00000518161.1:p.Met270Gly
ENST00000472832.3:c.808_809delinsGG	ENSP00000483066.2:p.Met270Gly
ENST00000688158.2:n.1543_1544delinsGG
ENST00000688922.2:c.*638_*639delinsGG	ENSP00000508742.2:n.*638_*639delinsGG
ENST00000700021.1:c.763_764delinsGG	ENSP00000514757.1:p.Met255Gly
ENST00000700022.1:c.*147_*148delinsGG	ENSP00000514758.1:n.*147_*148delinsGG
ENST00000700023.1:n.1966_1967delinsGG
ENST00000700024.1:n.2200_2201delinsGG
ENST00000700025.1:n.1577_1578delinsGG
ENST00000700026.1:n.445_446delinsGG
ENST00000700029.1:c.735_736delinsGG
ENST00000706954.1:c.808_809delinsGG	ENSP00000516674.1:p.Met270Gly
ENST00000706955.1:c.*843_*844delinsGG	ENSP00000516675.1:n.*843_*844delinsGG
ENST00000686459.1:c.*394_*395delinsGG	ENSP00000508909.1:n.*394_*395delinsGG
ENST00000688158.1:c.*919_*920delinsGG	ENSP00000509254.1:n.*919_*920delinsGG
ENST00000688308.1:c.808_809delinsGG	ENSP00000508752.1:p.Met270Gly
ENST00000688922.1:c.729_730delinsGG
ENST00000693560.1:c.1327_1328delinsGG	ENSP00000509861.1:p.Met443Gly
ENST00000371953.8:c.808_809delinsGG MANE Select	ENSP00000361021.3:p.Met270Gly
ENST00000371953.7:c.808_809delinsGG	ENSP00000361021.3:p.Met270Gly
ENST00000472832.2:c.235_236delinsGG	ENSP00000483066.1:p.Met79Gly
NM_000314.5:c.808_809delinsGG	NP_000305.3:p.Met270Gly
NM_000314.6:c.808_809delinsGG	NP_000305.3:p.Met270Gly
NM_001304717.2:c.1327_1328delinsGG	NP_001291646.2:p.Met443Gly
NM_001304718.1:c.217_218delinsGG	NP_001291647.1:p.Met73Gly
XM_006717926.2:c.763_764delinsGG	XP_006717989.1:p.Met255Gly
XM_011539981.1:c.808_809delinsGG	XP_011538283.1:p.Met270Gly
XM_011539982.1:c.712_713delinsGG	XP_011538284.1:p.Met238Gly
XR_945791.1:n.1378_1379delinsGG
NM_000314.7:c.808_809delinsGG	NP_000305.3:p.Met270Gly
NM_001304717.5:c.1327_1328delinsGG	NP_001291646.4:p.Met443Gly
NM_001304718.2:c.217_218delinsGG	NP_001291647.1:p.Met73Gly
NM_000314.8:c.808_809delinsGG MANE Select	NP_000305.3:p.Met270Gly