Canonical Allele Identifier: CA669572491

Gene: PTEN

Linked Data

• dbSNP Id: rs1196531575
• MyVariant Identifiers: chr10:g.87965013_87965014del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965015_87965016del , CM000672.2:g.87965015_87965016del	GRCh38
NC_000010.10:g.89724772_89724773del , CM000672.1:g.89724772_89724773del	GRCh37
NC_000010.9:g.89714752_89714753del	NCBI36
NG_007466.2:g.106577_106578del , LRG_311:g.106577_106578del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1120-272_1120-271del	ENSP00000514759.2:n.1120-272_1120-271del
ENST00000710265.1:c.*56-272_*56-271del	ENSP00000518161.1:n.*56-272_*56-271del
ENST00000688158.2:n.1762-272_1762-271del
ENST00000688922.2:c.*857-272_*857-271del	ENSP00000508742.2:n.*857-272_*857-271del
ENST00000700021.1:c.982-272_982-271del	ENSP00000514757.1:n.982-272_982-271del
ENST00000700022.1:c.*366-272_*366-271del	ENSP00000514758.1:n.*366-272_*366-271del
ENST00000700023.1:n.2185-272_2185-271del
ENST00000700024.1:n.2419-272_2419-271del
ENST00000706954.1:c.1027-272_1027-271del	ENSP00000516674.1:n.1027-272_1027-271del
ENST00000706955.1:c.*1062-272_*1062-271del	ENSP00000516675.1:n.*1062-272_*1062-271del
ENST00000686459.1:c.*613-272_*613-271del	ENSP00000508909.1:n.*613-272_*613-271del
ENST00000688158.1:c.*1138-272_*1138-271del	ENSP00000509254.1:n.*1138-272_*1138-271del
ENST00000688308.1:c.1027-272_1027-271del	ENSP00000508752.1:n.1027-272_1027-271del
ENST00000688922.1:c.948-272_948-271del
ENST00000693560.1:c.1546-272_1546-271del	ENSP00000509861.1:n.1546-272_1546-271del
ENST00000371953.8:c.1027-272_1027-271del MANE Select	ENSP00000361021.3:n.1027-272_1027-271del
ENST00000371953.7:c.1027-272_1027-271del	ENSP00000361021.3:n.1027-272_1027-271del
NM_000314.5:c.1027-272_1027-271del	NP_000305.3:n.1027-272_1027-271del
NM_000314.6:c.1027-272_1027-271del	NP_000305.3:n.1027-272_1027-271del
NM_001304717.2:c.1546-272_1546-271del	NP_001291646.2:n.1546-272_1546-271del
NM_001304718.1:c.436-272_436-271del	NP_001291647.1:n.436-272_436-271del
XM_006717926.2:c.982-272_982-271del	XP_006717989.1:n.982-272_982-271del
XM_011539982.1:c.931-272_931-271del	XP_011538284.1:n.931-272_931-271del
XR_945791.1:n.1597-272_1597-271del
NM_000314.7:c.1027-272_1027-271del	NP_000305.3:n.1027-272_1027-271del
NM_001304717.5:c.1546-272_1546-271del	NP_001291646.4:n.1546-272_1546-271del
NM_001304718.2:c.436-272_436-271del	NP_001291647.1:n.436-272_436-271del
NM_000314.8:c.1027-272_1027-271del MANE Select	NP_000305.3:n.1027-272_1027-271del