Canonical Allele Identifier: CA2610049804

Gene: PTEN

Linked Data

• gnomAD v4: 10-87966925-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966925_87966926insA , CM000672.2:g.87966925_87966926insA	GRCh38
NC_000010.10:g.89726682_89726683insA , CM000672.1:g.89726682_89726683insA	GRCh37
NC_000010.9:g.89716662_89716663insA	NCBI36
NG_007466.2:g.108487_108488insA , LRG_311:g.108487_108488insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1694_*1695insA	ENSP00000518161.1:n.*1694_*1695insA
ENST00000688158.2:n.3400_3401insA
ENST00000706954.1:c.*1453_*1454insA	ENSP00000516674.1:n.*1453_*1454insA
ENST00000706955.1:c.*2700_*2701insA	ENSP00000516675.1:n.*2700_*2701insA
ENST00000688158.1:c.*2776_*2777insA	ENSP00000509254.1:n.*2776_*2777insA
ENST00000693560.1:c.*1453_*1454insA	ENSP00000509861.1:n.*1453_*1454insA
ENST00000371953.8:c.*1453_*1454insA MANE Select	ENSP00000361021.3:n.*1453_*1454insA
ENST00000371953.7:c.*1453_*1454insA	ENSP00000361021.3:n.*1453_*1454insA
NM_000314.5:c.*1453_*1454insA	NP_000305.3:n.*1453_*1454insA
NM_000314.6:c.*1453_*1454insA	NP_000305.3:n.*1453_*1454insA
NM_001304717.2:c.*1453_*1454insA	NP_001291646.2:n.*1453_*1454insA
NM_001304718.1:c.*1453_*1454insA	NP_001291647.1:n.*1453_*1454insA
XM_006717926.2:c.*1453_*1454insA	XP_006717989.1:n.*1453_*1454insA
XM_011539982.1:c.*1453_*1454insA	XP_011538284.1:n.*1453_*1454insA
XR_945791.1:n.3235_3236insA
NM_000314.7:c.*1453_*1454insA	NP_000305.3:n.*1453_*1454insA
NM_001304717.5:c.*1453_*1454insA	NP_001291646.4:n.*1453_*1454insA
NM_001304718.2:c.*1453_*1454insA	NP_001291647.1:n.*1453_*1454insA
NM_000314.8:c.*1453_*1454insA MANE Select	NP_000305.3:n.*1453_*1454insA