Canonical Allele Identifier: CA891837394

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965345_87965346delinsTG , CM000672.2:g.87965345_87965346delinsTG	GRCh38
NC_000010.10:g.89725102_89725103delinsTG , CM000672.1:g.89725102_89725103delinsTG	GRCh37
NC_000010.9:g.89715082_89715083delinsTG	NCBI36
NG_007466.2:g.106907_106908delinsTG , LRG_311:g.106907_106908delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1178_1179delinsTG	ENSP00000514759.2:p.Ser393Leu
ENST00000710265.1:c.*114_*115delinsTG	ENSP00000518161.1:n.*114_*115delinsTG
ENST00000688158.2:n.1820_1821delinsTG
ENST00000688922.2:c.*915_*916delinsTG	ENSP00000508742.2:n.*915_*916delinsTG
ENST00000700021.1:c.1040_1041delinsTG	ENSP00000514757.1:p.Ser347Leu
ENST00000700022.1:c.*424_*425delinsTG	ENSP00000514758.1:n.*424_*425delinsTG
ENST00000700023.1:n.2243_2244delinsTG
ENST00000700024.1:n.2477_2478delinsTG
ENST00000706954.1:c.1085_1086delinsTG	ENSP00000516674.1:p.Ser362Leu
ENST00000706955.1:c.*1120_*1121delinsTG	ENSP00000516675.1:n.*1120_*1121delinsTG
ENST00000686459.1:c.*671_*672delinsTG	ENSP00000508909.1:n.*671_*672delinsTG
ENST00000688158.1:c.*1196_*1197delinsTG	ENSP00000509254.1:n.*1196_*1197delinsTG
ENST00000688308.1:c.1085_1086delinsTG	ENSP00000508752.1:p.Ser362Leu
ENST00000688922.1:c.1006_1007delinsTG
ENST00000693560.1:c.1604_1605delinsTG	ENSP00000509861.1:p.Ser535Leu
ENST00000371953.8:c.1085_1086delinsTG MANE Select	ENSP00000361021.3:p.Ser362Leu
ENST00000371953.7:c.1085_1086delinsTG	ENSP00000361021.3:p.Ser362Leu
NM_000314.5:c.1085_1086delinsTG	NP_000305.3:p.Ser362Leu
NM_000314.6:c.1085_1086delinsTG	NP_000305.3:p.Ser362Leu
NM_001304717.2:c.1604_1605delinsTG	NP_001291646.2:p.Ser535Leu
NM_001304718.1:c.494_495delinsTG	NP_001291647.1:p.Ser165Leu
XM_006717926.2:c.1040_1041delinsTG	XP_006717989.1:p.Ser347Leu
XM_011539982.1:c.989_990delinsTG	XP_011538284.1:p.Ser330Leu
XR_945791.1:n.1655_1656delinsTG
NM_000314.7:c.1085_1086delinsTG	NP_000305.3:p.Ser362Leu
NM_001304717.5:c.1604_1605delinsTG	NP_001291646.4:p.Ser535Leu
NM_001304718.2:c.494_495delinsTG	NP_001291647.1:p.Ser165Leu
NM_000314.8:c.1085_1086delinsTG MANE Select	NP_000305.3:p.Ser362Leu