Canonical Allele Identifier: CA2610049193

Gene: PTEN

Linked Data

• gnomAD v4: 10-87965473-A-ATT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965481_87965482dup , CM000672.2:g.87965481_87965482dup	GRCh38
NC_000010.10:g.89725238_89725239dup , CM000672.1:g.89725238_89725239dup	GRCh37
NC_000010.9:g.89715218_89715219dup	NCBI36
NG_007466.2:g.107043_107044dup , LRG_311:g.107043_107044dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.*9_*10dup	ENSP00000514759.2:n.*9_*10dup
ENST00000710265.1:c.*250_*251dup	ENSP00000518161.1:n.*250_*251dup
ENST00000688158.2:n.1956_1957dup
ENST00000688922.2:c.*1051_*1052dup	ENSP00000508742.2:n.*1051_*1052dup
ENST00000700021.1:c.*9_*10dup	ENSP00000514757.1:n.*9_*10dup
ENST00000700022.1:c.*560_*561dup	ENSP00000514758.1:n.*560_*561dup
ENST00000700023.1:n.2379_2380dup
ENST00000700024.1:n.2613_2614dup
ENST00000706954.1:c.*9_*10dup	ENSP00000516674.1:n.*9_*10dup
ENST00000706955.1:c.*1256_*1257dup	ENSP00000516675.1:n.*1256_*1257dup
ENST00000686459.1:c.*807_*808dup	ENSP00000508909.1:n.*807_*808dup
ENST00000688158.1:c.*1332_*1333dup	ENSP00000509254.1:n.*1332_*1333dup
ENST00000688308.1:c.*9_*10dup	ENSP00000508752.1:n.*9_*10dup
ENST00000688922.1:c.1142_1143dup
ENST00000693560.1:c.*9_*10dup	ENSP00000509861.1:n.*9_*10dup
ENST00000371953.8:c.*9_*10dup MANE Select	ENSP00000361021.3:n.*9_*10dup
ENST00000371953.7:c.*9_*10dup	ENSP00000361021.3:n.*9_*10dup
NM_000314.5:c.*9_*10dup	NP_000305.3:n.*9_*10dup
NM_000314.6:c.*9_*10dup	NP_000305.3:n.*9_*10dup
NM_001304717.2:c.*9_*10dup	NP_001291646.2:n.*9_*10dup
NM_001304718.1:c.*9_*10dup	NP_001291647.1:n.*9_*10dup
XM_006717926.2:c.*9_*10dup	XP_006717989.1:n.*9_*10dup
XM_011539982.1:c.*9_*10dup	XP_011538284.1:n.*9_*10dup
XR_945791.1:n.1791_1792dup
NM_000314.7:c.*9_*10dup	NP_000305.3:n.*9_*10dup
NM_001304717.5:c.*9_*10dup	NP_001291646.4:n.*9_*10dup
NM_001304718.2:c.*9_*10dup	NP_001291647.1:n.*9_*10dup
NM_000314.8:c.*9_*10dup MANE Select	NP_000305.3:n.*9_*10dup