Canonical Allele Identifier: CA594924153

Gene: PTEN

Linked Data

• gnomAD v2: 10-89726658-G-GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
• MyVariant Identifiers: chr10:g.89726658_89726659insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT (hg19) ; chr10:g.87966901_87966902insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966901_87966902insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000672.2:g.87966901_87966902insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh38
NC_000010.10:g.89726658_89726659insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000672.1:g.89726658_89726659insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh37
NC_000010.9:g.89716638_89716639insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NCBI36
NG_007466.2:g.108463_108464insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_311:g.108463_108464insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*1670_*1671insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000518161.1:n.*1670_*1671insTTTTTTT...
ENST00000688158.2:n.3376_3377insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000706954.1:c.*1429_*1430insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000516674.1:n.*1429_*1430insTTTTTTT...
ENST00000706955.1:c.*2676_*2677insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000516675.1:n.*2676_*2677insTTTTTTT...
ENST00000688158.1:c.*2752_*2753insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000509254.1:n.*2752_*2753insTTTTTTT...
ENST00000693560.1:c.*1429_*1430insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000509861.1:n.*1429_*1430insTTTTTTT...
ENST00000371953.8:c.*1429_*1430insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000361021.3:n.*1429_*1430insTTTTTTT...
ENST00000371953.7:c.*1429_*1430insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000361021.3:n.*1429_*1430insTTTTTTT...
NM_000314.5:c.*1429_*1430insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_000305.3:n.*1429_*1430insTTTTTTTTTTTTT...
NM_000314.6:c.*1429_*1430insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_000305.3:n.*1429_*1430insTTTTTTTTTTTTT...
NM_001304717.2:c.*1429_*1430insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001291646.2:n.*1429_*1430insTTTTTTTTTT...
NM_001304718.1:c.*1429_*1430insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001291647.1:n.*1429_*1430insTTTTTTTTTT...
XM_006717926.2:c.*1429_*1430insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_006717989.1:n.*1429_*1430insTTTTTTTTTT...
XM_011539982.1:c.*1429_*1430insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_011538284.1:n.*1429_*1430insTTTTTTTTTT...
XR_945791.1:n.3211_3212insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_000314.7:c.*1429_*1430insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_000305.3:n.*1429_*1430insTTTTTTTTTTTTT...
NM_001304717.5:c.*1429_*1430insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001291646.4:n.*1429_*1430insTTTTTTTTTT...
NM_001304718.2:c.*1429_*1430insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001291647.1:n.*1429_*1430insTTTTTTTTTT...
NM_000314.8:c.*1429_*1430insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	NP_000305.3:n.*1429_*1430insTTTTTTTTTTTTT...