Canonical Allele Identifier: CA891835768

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960993_87960994delinsAC , CM000672.2:g.87960993_87960994delinsAC	GRCh38
NC_000010.10:g.89720750_89720751delinsAC , CM000672.1:g.89720750_89720751delinsAC	GRCh37
NC_000010.9:g.89710730_89710731delinsAC	NCBI36
NG_007466.2:g.102555_102556delinsAC , LRG_311:g.102555_102556delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.994_995delinsAC	ENSP00000514759.2:p.Asp332Thr
ENST00000710265.1:c.901_902delinsAC	ENSP00000518161.1:p.Asp301Thr
ENST00000472832.3:c.901_902delinsAC	ENSP00000483066.2:p.Asp301Thr
ENST00000688158.2:n.1636_1637delinsAC
ENST00000688922.2:c.*731_*732delinsAC	ENSP00000508742.2:n.*731_*732delinsAC
ENST00000700021.1:c.856_857delinsAC	ENSP00000514757.1:p.Asp286Thr
ENST00000700022.1:c.*240_*241delinsAC	ENSP00000514758.1:n.*240_*241delinsAC
ENST00000700023.1:n.2059_2060delinsAC
ENST00000700024.1:n.2293_2294delinsAC
ENST00000700025.1:n.1670_1671delinsAC
ENST00000700026.1:n.538_539delinsAC
ENST00000706954.1:c.901_902delinsAC	ENSP00000516674.1:p.Asp301Thr
ENST00000706955.1:c.*936_*937delinsAC	ENSP00000516675.1:n.*936_*937delinsAC
ENST00000686459.1:c.*487_*488delinsAC	ENSP00000508909.1:n.*487_*488delinsAC
ENST00000688158.1:c.*1012_*1013delinsAC	ENSP00000509254.1:n.*1012_*1013delinsAC
ENST00000688308.1:c.901_902delinsAC	ENSP00000508752.1:p.Asp301Thr
ENST00000688922.1:c.822_823delinsAC
ENST00000693560.1:c.1420_1421delinsAC	ENSP00000509861.1:p.Asp474Thr
ENST00000371953.8:c.901_902delinsAC MANE Select	ENSP00000361021.3:p.Asp301Thr
ENST00000371953.7:c.901_902delinsAC	ENSP00000361021.3:p.Asp301Thr
ENST00000472832.2:c.328_329delinsAC	ENSP00000483066.1:p.Asp110Thr
NM_000314.5:c.901_902delinsAC	NP_000305.3:p.Asp301Thr
NM_000314.6:c.901_902delinsAC	NP_000305.3:p.Asp301Thr
NM_001304717.2:c.1420_1421delinsAC	NP_001291646.2:p.Asp474Thr
NM_001304718.1:c.310_311delinsAC	NP_001291647.1:p.Asp104Thr
XM_006717926.2:c.856_857delinsAC	XP_006717989.1:p.Asp286Thr
XM_011539981.1:c.901_902delinsAC	XP_011538283.1:p.Asp301Thr
XM_011539982.1:c.805_806delinsAC	XP_011538284.1:p.Asp269Thr
XR_945791.1:n.1471_1472delinsAC
NM_000314.7:c.901_902delinsAC	NP_000305.3:p.Asp301Thr
NM_001304717.5:c.1420_1421delinsAC	NP_001291646.4:p.Asp474Thr
NM_001304718.2:c.310_311delinsAC	NP_001291647.1:p.Asp104Thr
NM_000314.8:c.901_902delinsAC MANE Select	NP_000305.3:p.Asp301Thr