Canonical Allele Identifier: CA891837372

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965342_87965343delinsTG , CM000672.2:g.87965342_87965343delinsTG	GRCh38
NC_000010.10:g.89725099_89725100delinsTG , CM000672.1:g.89725099_89725100delinsTG	GRCh37
NC_000010.9:g.89715079_89715080delinsTG	NCBI36
NG_007466.2:g.106904_106905delinsTG , LRG_311:g.106904_106905delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1175_1176delinsTG	ENSP00000514759.2:p.Ser392Met
ENST00000710265.1:c.*111_*112delinsTG	ENSP00000518161.1:n.*111_*112delinsTG
ENST00000688158.2:n.1817_1818delinsTG
ENST00000688922.2:c.*912_*913delinsTG	ENSP00000508742.2:n.*912_*913delinsTG
ENST00000700021.1:c.1037_1038delinsTG	ENSP00000514757.1:p.Ser346Met
ENST00000700022.1:c.*421_*422delinsTG	ENSP00000514758.1:n.*421_*422delinsTG
ENST00000700023.1:n.2240_2241delinsTG
ENST00000700024.1:n.2474_2475delinsTG
ENST00000706954.1:c.1082_1083delinsTG	ENSP00000516674.1:p.Ser361Met
ENST00000706955.1:c.*1117_*1118delinsTG	ENSP00000516675.1:n.*1117_*1118delinsTG
ENST00000686459.1:c.*668_*669delinsTG	ENSP00000508909.1:n.*668_*669delinsTG
ENST00000688158.1:c.*1193_*1194delinsTG	ENSP00000509254.1:n.*1193_*1194delinsTG
ENST00000688308.1:c.1082_1083delinsTG	ENSP00000508752.1:p.Ser361Met
ENST00000688922.1:c.1003_1004delinsTG
ENST00000693560.1:c.1601_1602delinsTG	ENSP00000509861.1:p.Ser534Met
ENST00000371953.8:c.1082_1083delinsTG MANE Select	ENSP00000361021.3:p.Ser361Met
ENST00000371953.7:c.1082_1083delinsTG	ENSP00000361021.3:p.Ser361Met
NM_000314.5:c.1082_1083delinsTG	NP_000305.3:p.Ser361Met
NM_000314.6:c.1082_1083delinsTG	NP_000305.3:p.Ser361Met
NM_001304717.2:c.1601_1602delinsTG	NP_001291646.2:p.Ser534Met
NM_001304718.1:c.491_492delinsTG	NP_001291647.1:p.Ser164Met
XM_006717926.2:c.1037_1038delinsTG	XP_006717989.1:p.Ser346Met
XM_011539982.1:c.986_987delinsTG	XP_011538284.1:p.Ser329Met
XR_945791.1:n.1652_1653delinsTG
NM_000314.7:c.1082_1083delinsTG	NP_000305.3:p.Ser361Met
NM_001304717.5:c.1601_1602delinsTG	NP_001291646.4:p.Ser534Met
NM_001304718.2:c.491_492delinsTG	NP_001291647.1:p.Ser164Met
NM_000314.8:c.1082_1083delinsTG MANE Select	NP_000305.3:p.Ser361Met