Canonical Allele Identifier: CA891841126

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960969_87960970delinsAC , CM000672.2:g.87960969_87960970delinsAC	GRCh38
NC_000010.10:g.89720726_89720727delinsAC , CM000672.1:g.89720726_89720727delinsAC	GRCh37
NC_000010.9:g.89710706_89710707delinsAC	NCBI36
NG_007466.2:g.102531_102532delinsAC , LRG_311:g.102531_102532delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.970_971delinsAC	ENSP00000514759.2:p.Gly324Thr
ENST00000710265.1:c.877_878delinsAC	ENSP00000518161.1:p.Gly293Thr
ENST00000472832.3:c.877_878delinsAC	ENSP00000483066.2:p.Gly293Thr
ENST00000688158.2:n.1612_1613delinsAC
ENST00000688922.2:c.*707_*708delinsAC	ENSP00000508742.2:n.*707_*708delinsAC
ENST00000700021.1:c.832_833delinsAC	ENSP00000514757.1:p.Gly278Thr
ENST00000700022.1:c.*216_*217delinsAC	ENSP00000514758.1:n.*216_*217delinsAC
ENST00000700023.1:n.2035_2036delinsAC
ENST00000700024.1:n.2269_2270delinsAC
ENST00000700025.1:n.1646_1647delinsAC
ENST00000700026.1:n.514_515delinsAC
ENST00000700029.1:c.804_805delinsAC
ENST00000706954.1:c.877_878delinsAC	ENSP00000516674.1:p.Gly293Thr
ENST00000706955.1:c.*912_*913delinsAC	ENSP00000516675.1:n.*912_*913delinsAC
ENST00000686459.1:c.*463_*464delinsAC	ENSP00000508909.1:n.*463_*464delinsAC
ENST00000688158.1:c.*988_*989delinsAC	ENSP00000509254.1:n.*988_*989delinsAC
ENST00000688308.1:c.877_878delinsAC	ENSP00000508752.1:p.Gly293Thr
ENST00000688922.1:c.798_799delinsAC
ENST00000693560.1:c.1396_1397delinsAC	ENSP00000509861.1:p.Gly466Thr
ENST00000371953.8:c.877_878delinsAC MANE Select	ENSP00000361021.3:p.Gly293Thr
ENST00000371953.7:c.877_878delinsAC	ENSP00000361021.3:p.Gly293Thr
ENST00000472832.2:c.304_305delinsAC	ENSP00000483066.1:p.Gly102Thr
NM_000314.5:c.877_878delinsAC	NP_000305.3:p.Gly293Thr
NM_000314.6:c.877_878delinsAC	NP_000305.3:p.Gly293Thr
NM_001304717.2:c.1396_1397delinsAC	NP_001291646.2:p.Gly466Thr
NM_001304718.1:c.286_287delinsAC	NP_001291647.1:p.Gly96Thr
XM_006717926.2:c.832_833delinsAC	XP_006717989.1:p.Gly278Thr
XM_011539981.1:c.877_878delinsAC	XP_011538283.1:p.Gly293Thr
XM_011539982.1:c.781_782delinsAC	XP_011538284.1:p.Gly261Thr
XR_945791.1:n.1447_1448delinsAC
NM_000314.7:c.877_878delinsAC	NP_000305.3:p.Gly293Thr
NM_001304717.5:c.1396_1397delinsAC	NP_001291646.4:p.Gly466Thr
NM_001304718.2:c.286_287delinsAC	NP_001291647.1:p.Gly96Thr
NM_000314.8:c.877_878delinsAC MANE Select	NP_000305.3:p.Gly293Thr