Canonical Allele Identifier: CA891836895

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961083_87961085delinsATG , CM000672.2:g.87961083_87961085delinsATG	GRCh38
NC_000010.10:g.89720840_89720842delinsATG , CM000672.1:g.89720840_89720842delinsATG	GRCh37
NC_000010.9:g.89710820_89710822delinsATG	NCBI36
NG_007466.2:g.102645_102647delinsATG , LRG_311:g.102645_102647delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1084_1086delinsATG	ENSP00000514759.2:p.Asp362Met
ENST00000710265.1:c.991_993delinsATG	ENSP00000518161.1:p.Asp331Met
ENST00000472832.3:c.991_993delinsATG	ENSP00000483066.2:p.Asp331Met
ENST00000688158.2:n.1726_1728delinsATG
ENST00000688922.2:c.*821_*823delinsATG	ENSP00000508742.2:n.*821_*823delinsATG
ENST00000700021.1:c.946_948delinsATG	ENSP00000514757.1:p.Asp316Met
ENST00000700022.1:c.*330_*332delinsATG	ENSP00000514758.1:n.*330_*332delinsATG
ENST00000700023.1:n.2149_2151delinsATG
ENST00000700024.1:n.2383_2385delinsATG
ENST00000700025.1:n.1760_1762delinsATG
ENST00000700026.1:n.628_630delinsATG
ENST00000706954.1:c.991_993delinsATG	ENSP00000516674.1:p.Asp331Met
ENST00000706955.1:c.*1026_*1028delinsATG	ENSP00000516675.1:n.*1026_*1028delinsATG
ENST00000686459.1:c.*577_*579delinsATG	ENSP00000508909.1:n.*577_*579delinsATG
ENST00000688158.1:c.*1102_*1104delinsATG	ENSP00000509254.1:n.*1102_*1104delinsATG
ENST00000688308.1:c.991_993delinsATG	ENSP00000508752.1:p.Asp331Met
ENST00000688922.1:c.912_914delinsATG
ENST00000693560.1:c.1510_1512delinsATG	ENSP00000509861.1:p.Asp504Met
ENST00000371953.8:c.991_993delinsATG MANE Select	ENSP00000361021.3:p.Asp331Met
ENST00000371953.7:c.991_993delinsATG	ENSP00000361021.3:p.Asp331Met
ENST00000472832.2:c.418_420delinsATG	ENSP00000483066.1:p.Asp140Met
NM_000314.5:c.991_993delinsATG	NP_000305.3:p.Asp331Met
NM_000314.6:c.991_993delinsATG	NP_000305.3:p.Asp331Met
NM_001304717.2:c.1510_1512delinsATG	NP_001291646.2:p.Asp504Met
NM_001304718.1:c.400_402delinsATG	NP_001291647.1:p.Asp134Met
XM_006717926.2:c.946_948delinsATG	XP_006717989.1:p.Asp316Met
XM_011539981.1:c.991_993delinsATG	XP_011538283.1:p.Asp331Met
XM_011539982.1:c.895_897delinsATG	XP_011538284.1:p.Asp299Met
XR_945791.1:n.1561_1563delinsATG
NM_000314.7:c.991_993delinsATG	NP_000305.3:p.Asp331Met
NM_001304717.5:c.1510_1512delinsATG	NP_001291646.4:p.Asp504Met
NM_001304718.2:c.400_402delinsATG	NP_001291647.1:p.Asp134Met
NM_000314.8:c.991_993delinsATG MANE Select	NP_000305.3:p.Asp331Met