Canonical Allele Identifier: CA1926173043

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965213_87965214delinsTA , CM000672.2:g.87965213_87965214delinsTA	GRCh38
NC_000010.10:g.89724970_89724971delinsTA , CM000672.1:g.89724970_89724971delinsTA	GRCh37
NC_000010.9:g.89714950_89714951delinsTA	NCBI36
NG_007466.2:g.106775_106776delinsTA , LRG_311:g.106775_106776delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1120-74_1120-73delinsTA	ENSP00000514759.2:n.1120-74_1120-73delinsTA
ENST00000710265.1:c.*56-74_*56-73delinsTA	ENSP00000518161.1:n.*56-74_*56-73delinsTA
ENST00000688158.2:n.1762-74_1762-73delinsTA
ENST00000688922.2:c.*857-74_*857-73delinsTA	ENSP00000508742.2:n.*857-74_*857-73delinsTA
ENST00000700021.1:c.982-74_982-73delinsTA	ENSP00000514757.1:n.982-74_982-73delinsTA
ENST00000700022.1:c.*366-74_*366-73delinsTA	ENSP00000514758.1:n.*366-74_*366-73delinsTA
ENST00000700023.1:n.2185-74_2185-73delinsTA
ENST00000700024.1:n.2419-74_2419-73delinsTA
ENST00000706954.1:c.1027-74_1027-73delinsTA	ENSP00000516674.1:n.1027-74_1027-73delinsTA
ENST00000706955.1:c.*1062-74_*1062-73delinsTA	ENSP00000516675.1:n.*1062-74_*1062-73delinsTA
ENST00000686459.1:c.*613-74_*613-73delinsTA	ENSP00000508909.1:n.*613-74_*613-73delinsTA
ENST00000688158.1:c.*1138-74_*1138-73delinsTA	ENSP00000509254.1:n.*1138-74_*1138-73delinsTA
ENST00000688308.1:c.1027-74_1027-73delinsTA	ENSP00000508752.1:n.1027-74_1027-73delinsTA
ENST00000688922.1:c.948-74_948-73delinsTA
ENST00000693560.1:c.1546-74_1546-73delinsTA	ENSP00000509861.1:n.1546-74_1546-73delinsTA
ENST00000371953.8:c.1027-74_1027-73delinsTA MANE Select	ENSP00000361021.3:n.1027-74_1027-73delinsTA
ENST00000371953.7:c.1027-74_1027-73delinsTA	ENSP00000361021.3:n.1027-74_1027-73delinsTA
NM_000314.5:c.1027-74_1027-73delinsTA	NP_000305.3:n.1027-74_1027-73delinsTA
NM_000314.6:c.1027-74_1027-73delinsTA	NP_000305.3:n.1027-74_1027-73delinsTA
NM_001304717.2:c.1546-74_1546-73delinsTA	NP_001291646.2:n.1546-74_1546-73delinsTA
NM_001304718.1:c.436-74_436-73delinsTA	NP_001291647.1:n.436-74_436-73delinsTA
XM_006717926.2:c.982-74_982-73delinsTA	XP_006717989.1:n.982-74_982-73delinsTA
XM_011539982.1:c.931-74_931-73delinsTA	XP_011538284.1:n.931-74_931-73delinsTA
XR_945791.1:n.1597-74_1597-73delinsTA
NM_000314.7:c.1027-74_1027-73delinsTA	NP_000305.3:n.1027-74_1027-73delinsTA
NM_001304717.5:c.1546-74_1546-73delinsTA	NP_001291646.4:n.1546-74_1546-73delinsTA
NM_001304718.2:c.436-74_436-73delinsTA	NP_001291647.1:n.436-74_436-73delinsTA
NM_000314.8:c.1027-74_1027-73delinsTA MANE Select	NP_000305.3:n.1027-74_1027-73delinsTA