Canonical Allele Identifier: CA891835296

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960969_87960971delinsTGG , CM000672.2:g.87960969_87960971delinsTGG	GRCh38
NC_000010.10:g.89720726_89720728delinsTGG , CM000672.1:g.89720726_89720728delinsTGG	GRCh37
NC_000010.9:g.89710706_89710708delinsTGG	NCBI36
NG_007466.2:g.102531_102533delinsTGG , LRG_311:g.102531_102533delinsTGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.970_972delinsTGG	ENSP00000514759.2:p.Gly324Trp
ENST00000710265.1:c.877_879delinsTGG	ENSP00000518161.1:p.Gly293Trp
ENST00000472832.3:c.877_879delinsTGG	ENSP00000483066.2:p.Gly293Trp
ENST00000688158.2:n.1612_1614delinsTGG
ENST00000688922.2:c.*707_*709delinsTGG	ENSP00000508742.2:n.*707_*709delinsTGG
ENST00000700021.1:c.832_834delinsTGG	ENSP00000514757.1:p.Gly278Trp
ENST00000700022.1:c.*216_*218delinsTGG	ENSP00000514758.1:n.*216_*218delinsTGG
ENST00000700023.1:n.2035_2037delinsTGG
ENST00000700024.1:n.2269_2271delinsTGG
ENST00000700025.1:n.1646_1648delinsTGG
ENST00000700026.1:n.514_516delinsTGG
ENST00000700029.1:c.804_806delinsTGG
ENST00000706954.1:c.877_879delinsTGG	ENSP00000516674.1:p.Gly293Trp
ENST00000706955.1:c.*912_*914delinsTGG	ENSP00000516675.1:n.*912_*914delinsTGG
ENST00000686459.1:c.*463_*465delinsTGG	ENSP00000508909.1:n.*463_*465delinsTGG
ENST00000688158.1:c.*988_*990delinsTGG	ENSP00000509254.1:n.*988_*990delinsTGG
ENST00000688308.1:c.877_879delinsTGG	ENSP00000508752.1:p.Gly293Trp
ENST00000688922.1:c.798_800delinsTGG
ENST00000693560.1:c.1396_1398delinsTGG	ENSP00000509861.1:p.Gly466Trp
ENST00000371953.8:c.877_879delinsTGG MANE Select	ENSP00000361021.3:p.Gly293Trp
ENST00000371953.7:c.877_879delinsTGG	ENSP00000361021.3:p.Gly293Trp
ENST00000472832.2:c.304_306delinsTGG	ENSP00000483066.1:p.Gly102Trp
NM_000314.5:c.877_879delinsTGG	NP_000305.3:p.Gly293Trp
NM_000314.6:c.877_879delinsTGG	NP_000305.3:p.Gly293Trp
NM_001304717.2:c.1396_1398delinsTGG	NP_001291646.2:p.Gly466Trp
NM_001304718.1:c.286_288delinsTGG	NP_001291647.1:p.Gly96Trp
XM_006717926.2:c.832_834delinsTGG	XP_006717989.1:p.Gly278Trp
XM_011539981.1:c.877_879delinsTGG	XP_011538283.1:p.Gly293Trp
XM_011539982.1:c.781_783delinsTGG	XP_011538284.1:p.Gly261Trp
XR_945791.1:n.1447_1449delinsTGG
NM_000314.7:c.877_879delinsTGG	NP_000305.3:p.Gly293Trp
NM_001304717.5:c.1396_1398delinsTGG	NP_001291646.4:p.Gly466Trp
NM_001304718.2:c.286_288delinsTGG	NP_001291647.1:p.Gly96Trp
NM_000314.8:c.877_879delinsTGG MANE Select	NP_000305.3:p.Gly293Trp