Canonical Allele Identifier: CA930910850

Gene: PTEN

Linked Data

• gnomAD v3: 10-87966929-T-TA
• gnomAD v4: 10-87966929-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966929_87966930insA , CM000672.2:g.87966929_87966930insA	GRCh38
NC_000010.10:g.89726686_89726687insA , CM000672.1:g.89726686_89726687insA	GRCh37
NC_000010.9:g.89716666_89716667insA	NCBI36
NG_007466.2:g.108491_108492insA , LRG_311:g.108491_108492insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1698_*1699insA	ENSP00000518161.1:n.*1698_*1699insA
ENST00000688158.2:n.3404_3405insA
ENST00000706954.1:c.*1457_*1458insA	ENSP00000516674.1:n.*1457_*1458insA
ENST00000706955.1:c.*2704_*2705insA	ENSP00000516675.1:n.*2704_*2705insA
ENST00000688158.1:c.*2780_*2781insA	ENSP00000509254.1:n.*2780_*2781insA
ENST00000693560.1:c.*1457_*1458insA	ENSP00000509861.1:n.*1457_*1458insA
ENST00000371953.8:c.*1457_*1458insA MANE Select	ENSP00000361021.3:n.*1457_*1458insA
ENST00000371953.7:c.*1457_*1458insA	ENSP00000361021.3:n.*1457_*1458insA
NM_000314.5:c.*1457_*1458insA	NP_000305.3:n.*1457_*1458insA
NM_000314.6:c.*1457_*1458insA	NP_000305.3:n.*1457_*1458insA
NM_001304717.2:c.*1457_*1458insA	NP_001291646.2:n.*1457_*1458insA
NM_001304718.1:c.*1457_*1458insA	NP_001291647.1:n.*1457_*1458insA
XM_006717926.2:c.*1457_*1458insA	XP_006717989.1:n.*1457_*1458insA
XM_011539982.1:c.*1457_*1458insA	XP_011538284.1:n.*1457_*1458insA
XR_945791.1:n.3239_3240insA
NM_000314.7:c.*1457_*1458insA	NP_000305.3:n.*1457_*1458insA
NM_001304717.5:c.*1457_*1458insA	NP_001291646.4:n.*1457_*1458insA
NM_001304718.2:c.*1457_*1458insA	NP_001291647.1:n.*1457_*1458insA
NM_000314.8:c.*1457_*1458insA MANE Select	NP_000305.3:n.*1457_*1458insA