Canonical Allele Identifier: CA594924156

Gene: PTEN

Linked Data

• dbSNP Id: rs1564571439
• gnomAD v2: 10-89726658-G-GTT
• gnomAD v3: 10-87966901-G-GTT
• gnomAD v4: 10-87966901-G-GTT
• MyVariant Identifiers: chr10:g.89726658_89726659insTT (hg19) ; chr10:g.87966901_87966902insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966901_87966902insTT , CM000672.2:g.87966901_87966902insTT	GRCh38
NC_000010.10:g.89726658_89726659insTT , CM000672.1:g.89726658_89726659insTT	GRCh37
NC_000010.9:g.89716638_89716639insTT	NCBI36
NG_007466.2:g.108463_108464insTT , LRG_311:g.108463_108464insTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*1670_*1671insTT	ENSP00000518161.1:n.*1670_*1671insTT
ENST00000688158.2:n.3376_3377insTT
ENST00000706954.1:c.*1429_*1430insTT	ENSP00000516674.1:n.*1429_*1430insTT
ENST00000706955.1:c.*2676_*2677insTT	ENSP00000516675.1:n.*2676_*2677insTT
ENST00000688158.1:c.*2752_*2753insTT	ENSP00000509254.1:n.*2752_*2753insTT
ENST00000693560.1:c.*1429_*1430insTT	ENSP00000509861.1:n.*1429_*1430insTT
ENST00000371953.8:c.*1429_*1430insTT MANE Select	ENSP00000361021.3:n.*1429_*1430insTT
ENST00000371953.7:c.*1429_*1430insTT	ENSP00000361021.3:n.*1429_*1430insTT
NM_000314.5:c.*1429_*1430insTT	NP_000305.3:n.*1429_*1430insTT
NM_000314.6:c.*1429_*1430insTT	NP_000305.3:n.*1429_*1430insTT
NM_001304717.2:c.*1429_*1430insTT	NP_001291646.2:n.*1429_*1430insTT
NM_001304718.1:c.*1429_*1430insTT	NP_001291647.1:n.*1429_*1430insTT
XM_006717926.2:c.*1429_*1430insTT	XP_006717989.1:n.*1429_*1430insTT
XM_011539982.1:c.*1429_*1430insTT	XP_011538284.1:n.*1429_*1430insTT
XR_945791.1:n.3211_3212insTT
NM_000314.7:c.*1429_*1430insTT	NP_000305.3:n.*1429_*1430insTT
NM_001304717.5:c.*1429_*1430insTT	NP_001291646.4:n.*1429_*1430insTT
NM_001304718.2:c.*1429_*1430insTT	NP_001291647.1:n.*1429_*1430insTT
NM_000314.8:c.*1429_*1430insTT MANE Select	NP_000305.3:n.*1429_*1430insTT