Canonical Allele Identifier: CA891837682

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965380_87965382delinsTGG , CM000672.2:g.87965380_87965382delinsTGG	GRCh38
NC_000010.10:g.89725137_89725139delinsTGG , CM000672.1:g.89725137_89725139delinsTGG	GRCh37
NC_000010.9:g.89715117_89715119delinsTGG	NCBI36
NG_007466.2:g.106942_106944delinsTGG , LRG_311:g.106942_106944delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1213_1215delinsTGG	ENSP00000514759.2:p.Pro405Trp
ENST00000710265.1:c.*149_*151delinsTGG	ENSP00000518161.1:n.*149_*151delinsTGG
ENST00000688158.2:n.1855_1857delinsTGG
ENST00000688922.2:c.*950_*952delinsTGG	ENSP00000508742.2:n.*950_*952delinsTGG
ENST00000700021.1:c.1075_1077delinsTGG	ENSP00000514757.1:p.Pro359Trp
ENST00000700022.1:c.*459_*461delinsTGG	ENSP00000514758.1:n.*459_*461delinsTGG
ENST00000700023.1:n.2278_2280delinsTGG
ENST00000700024.1:n.2512_2514delinsTGG
ENST00000706954.1:c.1120_1122delinsTGG	ENSP00000516674.1:p.Pro374Trp
ENST00000706955.1:c.*1155_*1157delinsTGG	ENSP00000516675.1:n.*1155_*1157delinsTGG
ENST00000686459.1:c.*706_*708delinsTGG	ENSP00000508909.1:n.*706_*708delinsTGG
ENST00000688158.1:c.*1231_*1233delinsTGG	ENSP00000509254.1:n.*1231_*1233delinsTGG
ENST00000688308.1:c.1120_1122delinsTGG	ENSP00000508752.1:p.Pro374Trp
ENST00000688922.1:c.1041_1043delinsTGG
ENST00000693560.1:c.1639_1641delinsTGG	ENSP00000509861.1:p.Pro547Trp
ENST00000371953.8:c.1120_1122delinsTGG MANE Select	ENSP00000361021.3:p.Pro374Trp
ENST00000371953.7:c.1120_1122delinsTGG	ENSP00000361021.3:p.Pro374Trp
NM_000314.5:c.1120_1122delinsTGG	NP_000305.3:p.Pro374Trp
NM_000314.6:c.1120_1122delinsTGG	NP_000305.3:p.Pro374Trp
NM_001304717.2:c.1639_1641delinsTGG	NP_001291646.2:p.Pro547Trp
NM_001304718.1:c.529_531delinsTGG	NP_001291647.1:p.Pro177Trp
XM_006717926.2:c.1075_1077delinsTGG	XP_006717989.1:p.Pro359Trp
XM_011539982.1:c.1024_1026delinsTGG	XP_011538284.1:p.Pro342Trp
XR_945791.1:n.1690_1692delinsTGG
NM_000314.7:c.1120_1122delinsTGG	NP_000305.3:p.Pro374Trp
NM_001304717.5:c.1639_1641delinsTGG	NP_001291646.4:p.Pro547Trp
NM_001304718.2:c.529_531delinsTGG	NP_001291647.1:p.Pro177Trp
NM_000314.8:c.1120_1122delinsTGG MANE Select	NP_000305.3:p.Pro374Trp