Canonical Allele Identifier: CA1926172829

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965012_87965014delinsCAG , CM000672.2:g.87965012_87965014delinsCAG	GRCh38
NC_000010.10:g.89724769_89724771delinsCAG , CM000672.1:g.89724769_89724771delinsCAG	GRCh37
NC_000010.9:g.89714749_89714751delinsCAG	NCBI36
NG_007466.2:g.106574_106576delinsCAG , LRG_311:g.106574_106576delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1120-275_1120-273delinsCAG	ENSP00000514759.2:n.1120-275_1120-273delinsCAG
ENST00000710265.1:c.*56-275_*56-273delinsCAG	ENSP00000518161.1:n.*56-275_*56-273delinsCAG
ENST00000688158.2:n.1762-275_1762-273delinsCAG
ENST00000688922.2:c.*857-275_*857-273delinsCAG	ENSP00000508742.2:n.*857-275_*857-273delinsCAG
ENST00000700021.1:c.982-275_982-273delinsCAG	ENSP00000514757.1:n.982-275_982-273delinsCAG
ENST00000700022.1:c.*366-275_*366-273delinsCAG	ENSP00000514758.1:n.*366-275_*366-273delinsCAG
ENST00000700023.1:n.2185-275_2185-273delinsCAG
ENST00000700024.1:n.2419-275_2419-273delinsCAG
ENST00000706954.1:c.1027-275_1027-273delinsCAG	ENSP00000516674.1:n.1027-275_1027-273delinsCAG
ENST00000706955.1:c.*1062-275_*1062-273delinsCAG	ENSP00000516675.1:n.*1062-275_*1062-273delinsCAG
ENST00000686459.1:c.*613-275_*613-273delinsCAG	ENSP00000508909.1:n.*613-275_*613-273delinsCAG
ENST00000688158.1:c.*1138-275_*1138-273delinsCAG	ENSP00000509254.1:n.*1138-275_*1138-273delinsCAG
ENST00000688308.1:c.1027-275_1027-273delinsCAG	ENSP00000508752.1:n.1027-275_1027-273delinsCAG
ENST00000688922.1:c.948-275_948-273delinsCAG
ENST00000693560.1:c.1546-275_1546-273delinsCAG	ENSP00000509861.1:n.1546-275_1546-273delinsCAG
ENST00000371953.8:c.1027-275_1027-273delinsCAG MANE Select	ENSP00000361021.3:n.1027-275_1027-273delinsCAG
ENST00000371953.7:c.1027-275_1027-273delinsCAG	ENSP00000361021.3:n.1027-275_1027-273delinsCAG
NM_000314.5:c.1027-275_1027-273delinsCAG	NP_000305.3:n.1027-275_1027-273delinsCAG
NM_000314.6:c.1027-275_1027-273delinsCAG	NP_000305.3:n.1027-275_1027-273delinsCAG
NM_001304717.2:c.1546-275_1546-273delinsCAG	NP_001291646.2:n.1546-275_1546-273delinsCAG
NM_001304718.1:c.436-275_436-273delinsCAG	NP_001291647.1:n.436-275_436-273delinsCAG
XM_006717926.2:c.982-275_982-273delinsCAG	XP_006717989.1:n.982-275_982-273delinsCAG
XM_011539982.1:c.931-275_931-273delinsCAG	XP_011538284.1:n.931-275_931-273delinsCAG
XR_945791.1:n.1597-275_1597-273delinsCAG
NM_000314.7:c.1027-275_1027-273delinsCAG	NP_000305.3:n.1027-275_1027-273delinsCAG
NM_001304717.5:c.1546-275_1546-273delinsCAG	NP_001291646.4:n.1546-275_1546-273delinsCAG
NM_001304718.2:c.436-275_436-273delinsCAG	NP_001291647.1:n.436-275_436-273delinsCAG
NM_000314.8:c.1027-275_1027-273delinsCAG MANE Select	NP_000305.3:n.1027-275_1027-273delinsCAG