Canonical Allele Identifier: CA891840232

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960910_87960911delinsAA , CM000672.2:g.87960910_87960911delinsAA	GRCh38
NC_000010.10:g.89720667_89720668delinsAA , CM000672.1:g.89720667_89720668delinsAA	GRCh37
NC_000010.9:g.89710647_89710648delinsAA	NCBI36
NG_007466.2:g.102472_102473delinsAA , LRG_311:g.102472_102473delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.911_912delinsAA	ENSP00000514759.2:p.Phe304Ter
ENST00000710265.1:c.818_819delinsAA	ENSP00000518161.1:p.Phe273Ter
ENST00000472832.3:c.818_819delinsAA	ENSP00000483066.2:p.Phe273Ter
ENST00000688158.2:n.1553_1554delinsAA
ENST00000688922.2:c.*648_*649delinsAA	ENSP00000508742.2:n.*648_*649delinsAA
ENST00000700021.1:c.773_774delinsAA	ENSP00000514757.1:p.Phe258Ter
ENST00000700022.1:c.*157_*158delinsAA	ENSP00000514758.1:n.*157_*158delinsAA
ENST00000700023.1:n.1976_1977delinsAA
ENST00000700024.1:n.2210_2211delinsAA
ENST00000700025.1:n.1587_1588delinsAA
ENST00000700026.1:n.455_456delinsAA
ENST00000700029.1:c.745_746delinsAA
ENST00000706954.1:c.818_819delinsAA	ENSP00000516674.1:p.Phe273Ter
ENST00000706955.1:c.*853_*854delinsAA	ENSP00000516675.1:n.*853_*854delinsAA
ENST00000686459.1:c.*404_*405delinsAA	ENSP00000508909.1:n.*404_*405delinsAA
ENST00000688158.1:c.*929_*930delinsAA	ENSP00000509254.1:n.*929_*930delinsAA
ENST00000688308.1:c.818_819delinsAA	ENSP00000508752.1:p.Phe273Ter
ENST00000688922.1:c.739_740delinsAA
ENST00000693560.1:c.1337_1338delinsAA	ENSP00000509861.1:p.Phe446Ter
ENST00000371953.8:c.818_819delinsAA MANE Select	ENSP00000361021.3:p.Phe273Ter
ENST00000371953.7:c.818_819delinsAA	ENSP00000361021.3:p.Phe273Ter
ENST00000472832.2:c.245_246delinsAA	ENSP00000483066.1:p.Phe82Ter
NM_000314.5:c.818_819delinsAA	NP_000305.3:p.Phe273Ter
NM_000314.6:c.818_819delinsAA	NP_000305.3:p.Phe273Ter
NM_001304717.2:c.1337_1338delinsAA	NP_001291646.2:p.Phe446Ter
NM_001304718.1:c.227_228delinsAA	NP_001291647.1:p.Phe76Ter
XM_006717926.2:c.773_774delinsAA	XP_006717989.1:p.Phe258Ter
XM_011539981.1:c.818_819delinsAA	XP_011538283.1:p.Phe273Ter
XM_011539982.1:c.722_723delinsAA	XP_011538284.1:p.Phe241Ter
XR_945791.1:n.1388_1389delinsAA
NM_000314.7:c.818_819delinsAA	NP_000305.3:p.Phe273Ter
NM_001304717.5:c.1337_1338delinsAA	NP_001291646.4:p.Phe446Ter
NM_001304718.2:c.227_228delinsAA	NP_001291647.1:p.Phe76Ter
NM_000314.8:c.818_819delinsAA MANE Select	NP_000305.3:p.Phe273Ter