Canonical Allele Identifier: CA211258444

Gene: PTEN

Linked Data

• dbSNP Id: rs962891061
• MyVariant Identifiers: chr10:g.89724792_89724797del (hg19) ; chr10:g.87965035_87965040del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965042_87965047del , CM000672.2:g.87965042_87965047del	GRCh38
NC_000010.10:g.89724799_89724804del , CM000672.1:g.89724799_89724804del	GRCh37
NC_000010.9:g.89714779_89714784del	NCBI36
NG_007466.2:g.106604_106609del , LRG_311:g.106604_106609del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1120-245_1120-240del	ENSP00000514759.2:n.1120-245_1120-240del
ENST00000710265.1:c.*56-245_*56-240del	ENSP00000518161.1:n.*56-245_*56-240del
ENST00000688158.2:n.1762-245_1762-240del
ENST00000688922.2:c.*857-245_*857-240del	ENSP00000508742.2:n.*857-245_*857-240del
ENST00000700021.1:c.982-245_982-240del	ENSP00000514757.1:n.982-245_982-240del
ENST00000700022.1:c.*366-245_*366-240del	ENSP00000514758.1:n.*366-245_*366-240del
ENST00000700023.1:n.2185-245_2185-240del
ENST00000700024.1:n.2419-245_2419-240del
ENST00000706954.1:c.1027-245_1027-240del	ENSP00000516674.1:n.1027-245_1027-240del
ENST00000706955.1:c.*1062-245_*1062-240del	ENSP00000516675.1:n.*1062-245_*1062-240del
ENST00000686459.1:c.*613-245_*613-240del	ENSP00000508909.1:n.*613-245_*613-240del
ENST00000688158.1:c.*1138-245_*1138-240del	ENSP00000509254.1:n.*1138-245_*1138-240del
ENST00000688308.1:c.1027-245_1027-240del	ENSP00000508752.1:n.1027-245_1027-240del
ENST00000688922.1:c.948-245_948-240del
ENST00000693560.1:c.1546-245_1546-240del	ENSP00000509861.1:n.1546-245_1546-240del
ENST00000371953.8:c.1027-245_1027-240del MANE Select	ENSP00000361021.3:n.1027-245_1027-240del
ENST00000371953.7:c.1027-245_1027-240del	ENSP00000361021.3:n.1027-245_1027-240del
NM_000314.5:c.1027-245_1027-240del	NP_000305.3:n.1027-245_1027-240del
NM_000314.6:c.1027-245_1027-240del	NP_000305.3:n.1027-245_1027-240del
NM_001304717.2:c.1546-245_1546-240del	NP_001291646.2:n.1546-245_1546-240del
NM_001304718.1:c.436-245_436-240del	NP_001291647.1:n.436-245_436-240del
XM_006717926.2:c.982-245_982-240del	XP_006717989.1:n.982-245_982-240del
XM_011539982.1:c.931-245_931-240del	XP_011538284.1:n.931-245_931-240del
XR_945791.1:n.1597-245_1597-240del
NM_000314.7:c.1027-245_1027-240del	NP_000305.3:n.1027-245_1027-240del
NM_001304717.5:c.1546-245_1546-240del	NP_001291646.4:n.1546-245_1546-240del
NM_001304718.2:c.436-245_436-240del	NP_001291647.1:n.436-245_436-240del
NM_000314.8:c.1027-245_1027-240del MANE Select	NP_000305.3:n.1027-245_1027-240del