Canonical Allele Identifier: CA1926175697

Gene: PTEN

Linked Data

• dbSNP Id: rs1564571439

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966901_87966902insTTTT , CM000672.2:g.87966901_87966902insTTTT	GRCh38
NC_000010.10:g.89726658_89726659insTTTT , CM000672.1:g.89726658_89726659insTTTT	GRCh37
NC_000010.9:g.89716638_89716639insTTTT	NCBI36
NG_007466.2:g.108463_108464insTTTT , LRG_311:g.108463_108464insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1670_*1671insTTTT	ENSP00000518161.1:n.*1670_*1671insTTTT
ENST00000688158.2:n.3376_3377insTTTT
ENST00000706954.1:c.*1429_*1430insTTTT	ENSP00000516674.1:n.*1429_*1430insTTTT
ENST00000706955.1:c.*2676_*2677insTTTT	ENSP00000516675.1:n.*2676_*2677insTTTT
ENST00000688158.1:c.*2752_*2753insTTTT	ENSP00000509254.1:n.*2752_*2753insTTTT
ENST00000693560.1:c.*1429_*1430insTTTT	ENSP00000509861.1:n.*1429_*1430insTTTT
ENST00000371953.8:c.*1429_*1430insTTTT MANE Select	ENSP00000361021.3:n.*1429_*1430insTTTT
ENST00000371953.7:c.*1429_*1430insTTTT	ENSP00000361021.3:n.*1429_*1430insTTTT
NM_000314.5:c.*1429_*1430insTTTT	NP_000305.3:n.*1429_*1430insTTTT
NM_000314.6:c.*1429_*1430insTTTT	NP_000305.3:n.*1429_*1430insTTTT
NM_001304717.2:c.*1429_*1430insTTTT	NP_001291646.2:n.*1429_*1430insTTTT
NM_001304718.1:c.*1429_*1430insTTTT	NP_001291647.1:n.*1429_*1430insTTTT
XM_006717926.2:c.*1429_*1430insTTTT	XP_006717989.1:n.*1429_*1430insTTTT
XM_011539982.1:c.*1429_*1430insTTTT	XP_011538284.1:n.*1429_*1430insTTTT
XR_945791.1:n.3211_3212insTTTT
NM_000314.7:c.*1429_*1430insTTTT	NP_000305.3:n.*1429_*1430insTTTT
NM_001304717.5:c.*1429_*1430insTTTT	NP_001291646.4:n.*1429_*1430insTTTT
NM_001304718.2:c.*1429_*1430insTTTT	NP_001291647.1:n.*1429_*1430insTTTT
NM_000314.8:c.*1429_*1430insTTTT MANE Select	NP_000305.3:n.*1429_*1430insTTTT