Canonical Allele Identifier: CA891835294

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960969_87960971delinsAAT , CM000672.2:g.87960969_87960971delinsAAT	GRCh38
NC_000010.10:g.89720726_89720728delinsAAT , CM000672.1:g.89720726_89720728delinsAAT	GRCh37
NC_000010.9:g.89710706_89710708delinsAAT	NCBI36
NG_007466.2:g.102531_102533delinsAAT , LRG_311:g.102531_102533delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.970_972delinsAAT	ENSP00000514759.2:p.Gly324Asn
ENST00000710265.1:c.877_879delinsAAT	ENSP00000518161.1:p.Gly293Asn
ENST00000472832.3:c.877_879delinsAAT	ENSP00000483066.2:p.Gly293Asn
ENST00000688158.2:n.1612_1614delinsAAT
ENST00000688922.2:c.*707_*709delinsAAT	ENSP00000508742.2:n.*707_*709delinsAAT
ENST00000700021.1:c.832_834delinsAAT	ENSP00000514757.1:p.Gly278Asn
ENST00000700022.1:c.*216_*218delinsAAT	ENSP00000514758.1:n.*216_*218delinsAAT
ENST00000700023.1:n.2035_2037delinsAAT
ENST00000700024.1:n.2269_2271delinsAAT
ENST00000700025.1:n.1646_1648delinsAAT
ENST00000700026.1:n.514_516delinsAAT
ENST00000700029.1:c.804_806delinsAAT
ENST00000706954.1:c.877_879delinsAAT	ENSP00000516674.1:p.Gly293Asn
ENST00000706955.1:c.*912_*914delinsAAT	ENSP00000516675.1:n.*912_*914delinsAAT
ENST00000686459.1:c.*463_*465delinsAAT	ENSP00000508909.1:n.*463_*465delinsAAT
ENST00000688158.1:c.*988_*990delinsAAT	ENSP00000509254.1:n.*988_*990delinsAAT
ENST00000688308.1:c.877_879delinsAAT	ENSP00000508752.1:p.Gly293Asn
ENST00000688922.1:c.798_800delinsAAT
ENST00000693560.1:c.1396_1398delinsAAT	ENSP00000509861.1:p.Gly466Asn
ENST00000371953.8:c.877_879delinsAAT MANE Select	ENSP00000361021.3:p.Gly293Asn
ENST00000371953.7:c.877_879delinsAAT	ENSP00000361021.3:p.Gly293Asn
ENST00000472832.2:c.304_306delinsAAT	ENSP00000483066.1:p.Gly102Asn
NM_000314.5:c.877_879delinsAAT	NP_000305.3:p.Gly293Asn
NM_000314.6:c.877_879delinsAAT	NP_000305.3:p.Gly293Asn
NM_001304717.2:c.1396_1398delinsAAT	NP_001291646.2:p.Gly466Asn
NM_001304718.1:c.286_288delinsAAT	NP_001291647.1:p.Gly96Asn
XM_006717926.2:c.832_834delinsAAT	XP_006717989.1:p.Gly278Asn
XM_011539981.1:c.877_879delinsAAT	XP_011538283.1:p.Gly293Asn
XM_011539982.1:c.781_783delinsAAT	XP_011538284.1:p.Gly261Asn
XR_945791.1:n.1447_1449delinsAAT
NM_000314.7:c.877_879delinsAAT	NP_000305.3:p.Gly293Asn
NM_001304717.5:c.1396_1398delinsAAT	NP_001291646.4:p.Gly466Asn
NM_001304718.2:c.286_288delinsAAT	NP_001291647.1:p.Gly96Asn
NM_000314.8:c.877_879delinsAAT MANE Select	NP_000305.3:p.Gly293Asn