Canonical Allele Identifier: CA2610049144

Gene: PTEN

Linked Data

• gnomAD v4: 10-87965175-TTAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965178_87965180del , CM000672.2:g.87965178_87965180del	GRCh38
NC_000010.10:g.89724935_89724937del , CM000672.1:g.89724935_89724937del	GRCh37
NC_000010.9:g.89714915_89714917del	NCBI36
NG_007466.2:g.106740_106742del , LRG_311:g.106740_106742del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1120-109_1120-107del	ENSP00000514759.2:n.1120-109_1120-107del
ENST00000710265.1:c.*56-109_*56-107del	ENSP00000518161.1:n.*56-109_*56-107del
ENST00000688158.2:n.1762-109_1762-107del
ENST00000688922.2:c.*857-109_*857-107del	ENSP00000508742.2:n.*857-109_*857-107del
ENST00000700021.1:c.982-109_982-107del	ENSP00000514757.1:n.982-109_982-107del
ENST00000700022.1:c.*366-109_*366-107del	ENSP00000514758.1:n.*366-109_*366-107del
ENST00000700023.1:n.2185-109_2185-107del
ENST00000700024.1:n.2419-109_2419-107del
ENST00000706954.1:c.1027-109_1027-107del	ENSP00000516674.1:n.1027-109_1027-107del
ENST00000706955.1:c.*1062-109_*1062-107del	ENSP00000516675.1:n.*1062-109_*1062-107del
ENST00000686459.1:c.*613-109_*613-107del	ENSP00000508909.1:n.*613-109_*613-107del
ENST00000688158.1:c.*1138-109_*1138-107del	ENSP00000509254.1:n.*1138-109_*1138-107del
ENST00000688308.1:c.1027-109_1027-107del	ENSP00000508752.1:n.1027-109_1027-107del
ENST00000688922.1:c.948-109_948-107del
ENST00000693560.1:c.1546-109_1546-107del	ENSP00000509861.1:n.1546-109_1546-107del
ENST00000371953.8:c.1027-109_1027-107del MANE Select	ENSP00000361021.3:n.1027-109_1027-107del
ENST00000371953.7:c.1027-109_1027-107del	ENSP00000361021.3:n.1027-109_1027-107del
NM_000314.5:c.1027-109_1027-107del	NP_000305.3:n.1027-109_1027-107del
NM_000314.6:c.1027-109_1027-107del	NP_000305.3:n.1027-109_1027-107del
NM_001304717.2:c.1546-109_1546-107del	NP_001291646.2:n.1546-109_1546-107del
NM_001304718.1:c.436-109_436-107del	NP_001291647.1:n.436-109_436-107del
XM_006717926.2:c.982-109_982-107del	XP_006717989.1:n.982-109_982-107del
XM_011539982.1:c.931-109_931-107del	XP_011538284.1:n.931-109_931-107del
XR_945791.1:n.1597-109_1597-107del
NM_000314.7:c.1027-109_1027-107del	NP_000305.3:n.1027-109_1027-107del
NM_001304717.5:c.1546-109_1546-107del	NP_001291646.4:n.1546-109_1546-107del
NM_001304718.2:c.436-109_436-107del	NP_001291647.1:n.436-109_436-107del
NM_000314.8:c.1027-109_1027-107del MANE Select	NP_000305.3:n.1027-109_1027-107del