Canonical Allele Identifier: CA891837592

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965371_87965373delinsAAA , CM000672.2:g.87965371_87965373delinsAAA	GRCh38
NC_000010.10:g.89725128_89725130delinsAAA , CM000672.1:g.89725128_89725130delinsAAA	GRCh37
NC_000010.9:g.89715108_89715110delinsAAA	NCBI36
NG_007466.2:g.106933_106935delinsAAA , LRG_311:g.106933_106935delinsAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1204_1206delinsAAA	ENSP00000514759.2:p.Asp402Lys
ENST00000710265.1:c.*140_*142delinsAAA	ENSP00000518161.1:n.*140_*142delinsAAA
ENST00000688158.2:n.1846_1848delinsAAA
ENST00000688922.2:c.*941_*943delinsAAA	ENSP00000508742.2:n.*941_*943delinsAAA
ENST00000700021.1:c.1066_1068delinsAAA	ENSP00000514757.1:p.Asp356Lys
ENST00000700022.1:c.*450_*452delinsAAA	ENSP00000514758.1:n.*450_*452delinsAAA
ENST00000700023.1:n.2269_2271delinsAAA
ENST00000700024.1:n.2503_2505delinsAAA
ENST00000706954.1:c.1111_1113delinsAAA	ENSP00000516674.1:p.Asp371Lys
ENST00000706955.1:c.*1146_*1148delinsAAA	ENSP00000516675.1:n.*1146_*1148delinsAAA
ENST00000686459.1:c.*697_*699delinsAAA	ENSP00000508909.1:n.*697_*699delinsAAA
ENST00000688158.1:c.*1222_*1224delinsAAA	ENSP00000509254.1:n.*1222_*1224delinsAAA
ENST00000688308.1:c.1111_1113delinsAAA	ENSP00000508752.1:p.Asp371Lys
ENST00000688922.1:c.1032_1034delinsAAA
ENST00000693560.1:c.1630_1632delinsAAA	ENSP00000509861.1:p.Asp544Lys
ENST00000371953.8:c.1111_1113delinsAAA MANE Select	ENSP00000361021.3:p.Asp371Lys
ENST00000371953.7:c.1111_1113delinsAAA	ENSP00000361021.3:p.Asp371Lys
NM_000314.5:c.1111_1113delinsAAA	NP_000305.3:p.Asp371Lys
NM_000314.6:c.1111_1113delinsAAA	NP_000305.3:p.Asp371Lys
NM_001304717.2:c.1630_1632delinsAAA	NP_001291646.2:p.Asp544Lys
NM_001304718.1:c.520_522delinsAAA	NP_001291647.1:p.Asp174Lys
XM_006717926.2:c.1066_1068delinsAAA	XP_006717989.1:p.Asp356Lys
XM_011539982.1:c.1015_1017delinsAAA	XP_011538284.1:p.Asp339Lys
XR_945791.1:n.1681_1683delinsAAA
NM_000314.7:c.1111_1113delinsAAA	NP_000305.3:p.Asp371Lys
NM_001304717.5:c.1630_1632delinsAAA	NP_001291646.4:p.Asp544Lys
NM_001304718.2:c.520_522delinsAAA	NP_001291647.1:p.Asp174Lys
NM_000314.8:c.1111_1113delinsAAA MANE Select	NP_000305.3:p.Asp371Lys