Canonical Allele Identifier: CA2610049791

Gene: PTEN

Linked Data

• gnomAD v4: 10-87966861-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966862del , CM000672.2:g.87966862del	GRCh38
NC_000010.10:g.89726619del , CM000672.1:g.89726619del	GRCh37
NC_000010.9:g.89716599del	NCBI36
NG_007466.2:g.108424del , LRG_311:g.108424del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.*1390del	ENSP00000514759.2:n.*1390del
ENST00000710265.1:c.*1631del	ENSP00000518161.1:n.*1631del
ENST00000688158.2:n.3337del
ENST00000688922.2:c.*2432del	ENSP00000508742.2:n.*2432del
ENST00000700021.1:c.*1390del	ENSP00000514757.1:n.*1390del
ENST00000700024.1:n.3994del
ENST00000706954.1:c.*1390del	ENSP00000516674.1:n.*1390del
ENST00000706955.1:c.*2637del	ENSP00000516675.1:n.*2637del
ENST00000688158.1:c.*2713del	ENSP00000509254.1:n.*2713del
ENST00000688308.1:c.*1390del	ENSP00000508752.1:n.*1390del
ENST00000688922.1:c.2523del
ENST00000693560.1:c.*1390del	ENSP00000509861.1:n.*1390del
ENST00000371953.8:c.*1390del MANE Select	ENSP00000361021.3:n.*1390del
ENST00000371953.7:c.*1390del	ENSP00000361021.3:n.*1390del
NM_000314.5:c.*1390del	NP_000305.3:n.*1390del
NM_000314.6:c.*1390del	NP_000305.3:n.*1390del
NM_001304717.2:c.*1390del	NP_001291646.2:n.*1390del
NM_001304718.1:c.*1390del	NP_001291647.1:n.*1390del
XM_006717926.2:c.*1390del	XP_006717989.1:n.*1390del
XM_011539982.1:c.*1390del	XP_011538284.1:n.*1390del
XR_945791.1:n.3172del
NM_000314.7:c.*1390del	NP_000305.3:n.*1390del
NM_001304717.5:c.*1390del	NP_001291646.4:n.*1390del
NM_001304718.2:c.*1390del	NP_001291647.1:n.*1390del
NM_000314.8:c.*1390del MANE Select	NP_000305.3:n.*1390del