Canonical Allele Identifier: CA1926172815

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87964999_87965000delinsTC , CM000672.2:g.87964999_87965000delinsTC	GRCh38
NC_000010.10:g.89724756_89724757delinsTC , CM000672.1:g.89724756_89724757delinsTC	GRCh37
NC_000010.9:g.89714736_89714737delinsTC	NCBI36
NG_007466.2:g.106561_106562delinsTC , LRG_311:g.106561_106562delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1120-288_1120-287delinsTC	ENSP00000514759.2:n.1120-288_1120-287delinsTC
ENST00000710265.1:c.*56-288_*56-287delinsTC	ENSP00000518161.1:n.*56-288_*56-287delinsTC
ENST00000688158.2:n.1762-288_1762-287delinsTC
ENST00000688922.2:c.*857-288_*857-287delinsTC	ENSP00000508742.2:n.*857-288_*857-287delinsTC
ENST00000700021.1:c.982-288_982-287delinsTC	ENSP00000514757.1:n.982-288_982-287delinsTC
ENST00000700022.1:c.*366-288_*366-287delinsTC	ENSP00000514758.1:n.*366-288_*366-287delinsTC
ENST00000700023.1:n.2185-288_2185-287delinsTC
ENST00000700024.1:n.2419-288_2419-287delinsTC
ENST00000706954.1:c.1027-288_1027-287delinsTC	ENSP00000516674.1:n.1027-288_1027-287delinsTC
ENST00000706955.1:c.*1062-288_*1062-287delinsTC	ENSP00000516675.1:n.*1062-288_*1062-287delinsTC
ENST00000686459.1:c.*613-288_*613-287delinsTC	ENSP00000508909.1:n.*613-288_*613-287delinsTC
ENST00000688158.1:c.*1138-288_*1138-287delinsTC	ENSP00000509254.1:n.*1138-288_*1138-287delinsTC
ENST00000688308.1:c.1027-288_1027-287delinsTC	ENSP00000508752.1:n.1027-288_1027-287delinsTC
ENST00000688922.1:c.948-288_948-287delinsTC
ENST00000693560.1:c.1546-288_1546-287delinsTC	ENSP00000509861.1:n.1546-288_1546-287delinsTC
ENST00000371953.8:c.1027-288_1027-287delinsTC MANE Select	ENSP00000361021.3:n.1027-288_1027-287delinsTC
ENST00000371953.7:c.1027-288_1027-287delinsTC	ENSP00000361021.3:n.1027-288_1027-287delinsTC
NM_000314.5:c.1027-288_1027-287delinsTC	NP_000305.3:n.1027-288_1027-287delinsTC
NM_000314.6:c.1027-288_1027-287delinsTC	NP_000305.3:n.1027-288_1027-287delinsTC
NM_001304717.2:c.1546-288_1546-287delinsTC	NP_001291646.2:n.1546-288_1546-287delinsTC
NM_001304718.1:c.436-288_436-287delinsTC	NP_001291647.1:n.436-288_436-287delinsTC
XM_006717926.2:c.982-288_982-287delinsTC	XP_006717989.1:n.982-288_982-287delinsTC
XM_011539982.1:c.931-288_931-287delinsTC	XP_011538284.1:n.931-288_931-287delinsTC
XR_945791.1:n.1597-288_1597-287delinsTC
NM_000314.7:c.1027-288_1027-287delinsTC	NP_000305.3:n.1027-288_1027-287delinsTC
NM_001304717.5:c.1546-288_1546-287delinsTC	NP_001291646.4:n.1546-288_1546-287delinsTC
NM_001304718.2:c.436-288_436-287delinsTC	NP_001291647.1:n.436-288_436-287delinsTC
NM_000314.8:c.1027-288_1027-287delinsTC MANE Select	NP_000305.3:n.1027-288_1027-287delinsTC