Canonical Allele Identifier: CA891837633

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965374_87965376delinsTGG , CM000672.2:g.87965374_87965376delinsTGG	GRCh38
NC_000010.10:g.89725131_89725133delinsTGG , CM000672.1:g.89725131_89725133delinsTGG	GRCh37
NC_000010.9:g.89715111_89715113delinsTGG	NCBI36
NG_007466.2:g.106936_106938delinsTGG , LRG_311:g.106936_106938delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1207_1209delinsTGG	ENSP00000514759.2:p.Asn403Trp
ENST00000710265.1:c.*143_*145delinsTGG	ENSP00000518161.1:n.*143_*145delinsTGG
ENST00000688158.2:n.1849_1851delinsTGG
ENST00000688922.2:c.*944_*946delinsTGG	ENSP00000508742.2:n.*944_*946delinsTGG
ENST00000700021.1:c.1069_1071delinsTGG	ENSP00000514757.1:p.Asn357Trp
ENST00000700022.1:c.*453_*455delinsTGG	ENSP00000514758.1:n.*453_*455delinsTGG
ENST00000700023.1:n.2272_2274delinsTGG
ENST00000700024.1:n.2506_2508delinsTGG
ENST00000706954.1:c.1114_1116delinsTGG	ENSP00000516674.1:p.Asn372Trp
ENST00000706955.1:c.*1149_*1151delinsTGG	ENSP00000516675.1:n.*1149_*1151delinsTGG
ENST00000686459.1:c.*700_*702delinsTGG	ENSP00000508909.1:n.*700_*702delinsTGG
ENST00000688158.1:c.*1225_*1227delinsTGG	ENSP00000509254.1:n.*1225_*1227delinsTGG
ENST00000688308.1:c.1114_1116delinsTGG	ENSP00000508752.1:p.Asn372Trp
ENST00000688922.1:c.1035_1037delinsTGG
ENST00000693560.1:c.1633_1635delinsTGG	ENSP00000509861.1:p.Asn545Trp
ENST00000371953.8:c.1114_1116delinsTGG MANE Select	ENSP00000361021.3:p.Asn372Trp
ENST00000371953.7:c.1114_1116delinsTGG	ENSP00000361021.3:p.Asn372Trp
NM_000314.5:c.1114_1116delinsTGG	NP_000305.3:p.Asn372Trp
NM_000314.6:c.1114_1116delinsTGG	NP_000305.3:p.Asn372Trp
NM_001304717.2:c.1633_1635delinsTGG	NP_001291646.2:p.Asn545Trp
NM_001304718.1:c.523_525delinsTGG	NP_001291647.1:p.Asn175Trp
XM_006717926.2:c.1069_1071delinsTGG	XP_006717989.1:p.Asn357Trp
XM_011539982.1:c.1018_1020delinsTGG	XP_011538284.1:p.Asn340Trp
XR_945791.1:n.1684_1686delinsTGG
NM_000314.7:c.1114_1116delinsTGG	NP_000305.3:p.Asn372Trp
NM_001304717.5:c.1633_1635delinsTGG	NP_001291646.4:p.Asn545Trp
NM_001304718.2:c.523_525delinsTGG	NP_001291647.1:p.Asn175Trp
NM_000314.8:c.1114_1116delinsTGG MANE Select	NP_000305.3:p.Asn372Trp