Canonical Allele Identifier: CA891837672

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965380_87965382delinsTAA , CM000672.2:g.87965380_87965382delinsTAA	GRCh38
NC_000010.10:g.89725137_89725139delinsTAA , CM000672.1:g.89725137_89725139delinsTAA	GRCh37
NC_000010.9:g.89715117_89715119delinsTAA	NCBI36
NG_007466.2:g.106942_106944delinsTAA , LRG_311:g.106942_106944delinsTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1213_1215delinsTAA	ENSP00000514759.2:p.Pro405Ter
ENST00000710265.1:c.*149_*151delinsTAA	ENSP00000518161.1:n.*149_*151delinsTAA
ENST00000688158.2:n.1855_1857delinsTAA
ENST00000688922.2:c.*950_*952delinsTAA	ENSP00000508742.2:n.*950_*952delinsTAA
ENST00000700021.1:c.1075_1077delinsTAA	ENSP00000514757.1:p.Pro359Ter
ENST00000700022.1:c.*459_*461delinsTAA	ENSP00000514758.1:n.*459_*461delinsTAA
ENST00000700023.1:n.2278_2280delinsTAA
ENST00000700024.1:n.2512_2514delinsTAA
ENST00000706954.1:c.1120_1122delinsTAA	ENSP00000516674.1:p.Pro374Ter
ENST00000706955.1:c.*1155_*1157delinsTAA	ENSP00000516675.1:n.*1155_*1157delinsTAA
ENST00000686459.1:c.*706_*708delinsTAA	ENSP00000508909.1:n.*706_*708delinsTAA
ENST00000688158.1:c.*1231_*1233delinsTAA	ENSP00000509254.1:n.*1231_*1233delinsTAA
ENST00000688308.1:c.1120_1122delinsTAA	ENSP00000508752.1:p.Pro374Ter
ENST00000688922.1:c.1041_1043delinsTAA
ENST00000693560.1:c.1639_1641delinsTAA	ENSP00000509861.1:p.Pro547Ter
ENST00000371953.8:c.1120_1122delinsTAA MANE Select	ENSP00000361021.3:p.Pro374Ter
ENST00000371953.7:c.1120_1122delinsTAA	ENSP00000361021.3:p.Pro374Ter
NM_000314.5:c.1120_1122delinsTAA	NP_000305.3:p.Pro374Ter
NM_000314.6:c.1120_1122delinsTAA	NP_000305.3:p.Pro374Ter
NM_001304717.2:c.1639_1641delinsTAA	NP_001291646.2:p.Pro547Ter
NM_001304718.1:c.529_531delinsTAA	NP_001291647.1:p.Pro177Ter
XM_006717926.2:c.1075_1077delinsTAA	XP_006717989.1:p.Pro359Ter
XM_011539982.1:c.1024_1026delinsTAA	XP_011538284.1:p.Pro342Ter
XR_945791.1:n.1690_1692delinsTAA
NM_000314.7:c.1120_1122delinsTAA	NP_000305.3:p.Pro374Ter
NM_001304717.5:c.1639_1641delinsTAA	NP_001291646.4:p.Pro547Ter
NM_001304718.2:c.529_531delinsTAA	NP_001291647.1:p.Pro177Ter
NM_000314.8:c.1120_1122delinsTAA MANE Select	NP_000305.3:p.Pro374Ter