Canonical Allele Identifier: CA211258424

Gene: PTEN

Linked Data

• dbSNP Id: rs1007415286
• gnomAD v3: 10-87965024-CTT-C
• gnomAD v4: 10-87965024-CTT-C
• MyVariant Identifiers: chr10:g.89724782_89724783del (hg19) ; chr10:g.87965025_87965026del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965025_87965026del , CM000672.2:g.87965025_87965026del	GRCh38
NC_000010.10:g.89724782_89724783del , CM000672.1:g.89724782_89724783del	GRCh37
NC_000010.9:g.89714762_89714763del	NCBI36
NG_007466.2:g.106587_106588del , LRG_311:g.106587_106588del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1120-262_1120-261del	ENSP00000514759.2:n.1120-262_1120-261del
ENST00000710265.1:c.*56-262_*56-261del	ENSP00000518161.1:n.*56-262_*56-261del
ENST00000688158.2:n.1762-262_1762-261del
ENST00000688922.2:c.*857-262_*857-261del	ENSP00000508742.2:n.*857-262_*857-261del
ENST00000700021.1:c.982-262_982-261del	ENSP00000514757.1:n.982-262_982-261del
ENST00000700022.1:c.*366-262_*366-261del	ENSP00000514758.1:n.*366-262_*366-261del
ENST00000700023.1:n.2185-262_2185-261del
ENST00000700024.1:n.2419-262_2419-261del
ENST00000706954.1:c.1027-262_1027-261del	ENSP00000516674.1:n.1027-262_1027-261del
ENST00000706955.1:c.*1062-262_*1062-261del	ENSP00000516675.1:n.*1062-262_*1062-261del
ENST00000686459.1:c.*613-262_*613-261del	ENSP00000508909.1:n.*613-262_*613-261del
ENST00000688158.1:c.*1138-262_*1138-261del	ENSP00000509254.1:n.*1138-262_*1138-261del
ENST00000688308.1:c.1027-262_1027-261del	ENSP00000508752.1:n.1027-262_1027-261del
ENST00000688922.1:c.948-262_948-261del
ENST00000693560.1:c.1546-262_1546-261del	ENSP00000509861.1:n.1546-262_1546-261del
ENST00000371953.8:c.1027-262_1027-261del MANE Select	ENSP00000361021.3:n.1027-262_1027-261del
ENST00000371953.7:c.1027-262_1027-261del	ENSP00000361021.3:n.1027-262_1027-261del
NM_000314.5:c.1027-262_1027-261del	NP_000305.3:n.1027-262_1027-261del
NM_000314.6:c.1027-262_1027-261del	NP_000305.3:n.1027-262_1027-261del
NM_001304717.2:c.1546-262_1546-261del	NP_001291646.2:n.1546-262_1546-261del
NM_001304718.1:c.436-262_436-261del	NP_001291647.1:n.436-262_436-261del
XM_006717926.2:c.982-262_982-261del	XP_006717989.1:n.982-262_982-261del
XM_011539982.1:c.931-262_931-261del	XP_011538284.1:n.931-262_931-261del
XR_945791.1:n.1597-262_1597-261del
NM_000314.7:c.1027-262_1027-261del	NP_000305.3:n.1027-262_1027-261del
NM_001304717.5:c.1546-262_1546-261del	NP_001291646.4:n.1546-262_1546-261del
NM_001304718.2:c.436-262_436-261del	NP_001291647.1:n.436-262_436-261del
NM_000314.8:c.1027-262_1027-261del MANE Select	NP_000305.3:n.1027-262_1027-261del