Canonical Allele Identifier: CA891835290

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960969_87960971delinsCAT , CM000672.2:g.87960969_87960971delinsCAT	GRCh38
NC_000010.10:g.89720726_89720728delinsCAT , CM000672.1:g.89720726_89720728delinsCAT	GRCh37
NC_000010.9:g.89710706_89710708delinsCAT	NCBI36
NG_007466.2:g.102531_102533delinsCAT , LRG_311:g.102531_102533delinsCAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.970_972delinsCAT	ENSP00000514759.2:p.Gly324His
ENST00000710265.1:c.877_879delinsCAT	ENSP00000518161.1:p.Gly293His
ENST00000472832.3:c.877_879delinsCAT	ENSP00000483066.2:p.Gly293His
ENST00000688158.2:n.1612_1614delinsCAT
ENST00000688922.2:c.*707_*709delinsCAT	ENSP00000508742.2:n.*707_*709delinsCAT
ENST00000700021.1:c.832_834delinsCAT	ENSP00000514757.1:p.Gly278His
ENST00000700022.1:c.*216_*218delinsCAT	ENSP00000514758.1:n.*216_*218delinsCAT
ENST00000700023.1:n.2035_2037delinsCAT
ENST00000700024.1:n.2269_2271delinsCAT
ENST00000700025.1:n.1646_1648delinsCAT
ENST00000700026.1:n.514_516delinsCAT
ENST00000700029.1:c.804_806delinsCAT
ENST00000706954.1:c.877_879delinsCAT	ENSP00000516674.1:p.Gly293His
ENST00000706955.1:c.*912_*914delinsCAT	ENSP00000516675.1:n.*912_*914delinsCAT
ENST00000686459.1:c.*463_*465delinsCAT	ENSP00000508909.1:n.*463_*465delinsCAT
ENST00000688158.1:c.*988_*990delinsCAT	ENSP00000509254.1:n.*988_*990delinsCAT
ENST00000688308.1:c.877_879delinsCAT	ENSP00000508752.1:p.Gly293His
ENST00000688922.1:c.798_800delinsCAT
ENST00000693560.1:c.1396_1398delinsCAT	ENSP00000509861.1:p.Gly466His
ENST00000371953.8:c.877_879delinsCAT MANE Select	ENSP00000361021.3:p.Gly293His
ENST00000371953.7:c.877_879delinsCAT	ENSP00000361021.3:p.Gly293His
ENST00000472832.2:c.304_306delinsCAT	ENSP00000483066.1:p.Gly102His
NM_000314.5:c.877_879delinsCAT	NP_000305.3:p.Gly293His
NM_000314.6:c.877_879delinsCAT	NP_000305.3:p.Gly293His
NM_001304717.2:c.1396_1398delinsCAT	NP_001291646.2:p.Gly466His
NM_001304718.1:c.286_288delinsCAT	NP_001291647.1:p.Gly96His
XM_006717926.2:c.832_834delinsCAT	XP_006717989.1:p.Gly278His
XM_011539981.1:c.877_879delinsCAT	XP_011538283.1:p.Gly293His
XM_011539982.1:c.781_783delinsCAT	XP_011538284.1:p.Gly261His
XR_945791.1:n.1447_1449delinsCAT
NM_000314.7:c.877_879delinsCAT	NP_000305.3:p.Gly293His
NM_001304717.5:c.1396_1398delinsCAT	NP_001291646.4:p.Gly466His
NM_001304718.2:c.286_288delinsCAT	NP_001291647.1:p.Gly96His
NM_000314.8:c.877_879delinsCAT MANE Select	NP_000305.3:p.Gly293His