Canonical Allele Identifier: CA918726303

Gene: PTEN

Linked Data

• dbSNP Id: rs1589298450
• gnomAD v4: 10-87967873-A-ATG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967873_87967874insTG , CM000672.2:g.87967873_87967874insTG	GRCh38
NC_000010.10:g.89727630_89727631insTG , CM000672.1:g.89727630_89727631insTG	GRCh37
NC_000010.9:g.89717610_89717611insTG	NCBI36
NG_007466.2:g.109435_109436insTG , LRG_311:g.109435_109436insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*2642_*2643insTG	ENSP00000518161.1:n.*2642_*2643insTG
ENST00000688158.2:n.4348_4349insTG
ENST00000706954.1:c.*2401_*2402insTG	ENSP00000516674.1:n.*2401_*2402insTG
ENST00000706955.1:c.*3648_*3649insTG	ENSP00000516675.1:n.*3648_*3649insTG
ENST00000688158.1:c.*3724_*3725insTG	ENSP00000509254.1:n.*3724_*3725insTG
ENST00000693560.1:c.*2401_*2402insTG	ENSP00000509861.1:n.*2401_*2402insTG
ENST00000371953.8:c.*2401_*2402insTG MANE Select	ENSP00000361021.3:n.*2401_*2402insTG
ENST00000371953.7:c.*2401_*2402insTG	ENSP00000361021.3:n.*2401_*2402insTG
NM_000314.5:c.*2401_*2402insTG	NP_000305.3:n.*2401_*2402insTG
NM_000314.6:c.*2401_*2402insTG	NP_000305.3:n.*2401_*2402insTG
NM_001304717.2:c.*2401_*2402insTG	NP_001291646.2:n.*2401_*2402insTG
NM_001304718.1:c.*2401_*2402insTG	NP_001291647.1:n.*2401_*2402insTG
XM_006717926.2:c.*2401_*2402insTG	XP_006717989.1:n.*2401_*2402insTG
XM_011539982.1:c.*2401_*2402insTG	XP_011538284.1:n.*2401_*2402insTG
XR_945791.1:n.4183_4184insTG
NM_000314.7:c.*2401_*2402insTG	NP_000305.3:n.*2401_*2402insTG
NM_001304717.5:c.*2401_*2402insTG	NP_001291646.4:n.*2401_*2402insTG
NM_001304718.2:c.*2401_*2402insTG	NP_001291647.1:n.*2401_*2402insTG
NM_000314.8:c.*2401_*2402insTG MANE Select	NP_000305.3:n.*2401_*2402insTG