Canonical Allele Identifier: CA891837708

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965383_87965385delinsAGA , CM000672.2:g.87965383_87965385delinsAGA	GRCh38
NC_000010.10:g.89725140_89725142delinsAGA , CM000672.1:g.89725140_89725142delinsAGA	GRCh37
NC_000010.9:g.89715120_89715122delinsAGA	NCBI36
NG_007466.2:g.106945_106947delinsAGA , LRG_311:g.106945_106947delinsAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1216_1218delinsAGA	ENSP00000514759.2:p.Asp406Arg
ENST00000710265.1:c.*152_*154delinsAGA	ENSP00000518161.1:n.*152_*154delinsAGA
ENST00000688158.2:n.1858_1860delinsAGA
ENST00000688922.2:c.*953_*955delinsAGA	ENSP00000508742.2:n.*953_*955delinsAGA
ENST00000700021.1:c.1078_1080delinsAGA	ENSP00000514757.1:p.Asp360Arg
ENST00000700022.1:c.*462_*464delinsAGA	ENSP00000514758.1:n.*462_*464delinsAGA
ENST00000700023.1:n.2281_2283delinsAGA
ENST00000700024.1:n.2515_2517delinsAGA
ENST00000706954.1:c.1123_1125delinsAGA	ENSP00000516674.1:p.Asp375Arg
ENST00000706955.1:c.*1158_*1160delinsAGA	ENSP00000516675.1:n.*1158_*1160delinsAGA
ENST00000686459.1:c.*709_*711delinsAGA	ENSP00000508909.1:n.*709_*711delinsAGA
ENST00000688158.1:c.*1234_*1236delinsAGA	ENSP00000509254.1:n.*1234_*1236delinsAGA
ENST00000688308.1:c.1123_1125delinsAGA	ENSP00000508752.1:p.Asp375Arg
ENST00000688922.1:c.1044_1046delinsAGA
ENST00000693560.1:c.1642_1644delinsAGA	ENSP00000509861.1:p.Asp548Arg
ENST00000371953.8:c.1123_1125delinsAGA MANE Select	ENSP00000361021.3:p.Asp375Arg
ENST00000371953.7:c.1123_1125delinsAGA	ENSP00000361021.3:p.Asp375Arg
NM_000314.5:c.1123_1125delinsAGA	NP_000305.3:p.Asp375Arg
NM_000314.6:c.1123_1125delinsAGA	NP_000305.3:p.Asp375Arg
NM_001304717.2:c.1642_1644delinsAGA	NP_001291646.2:p.Asp548Arg
NM_001304718.1:c.532_534delinsAGA	NP_001291647.1:p.Asp178Arg
XM_006717926.2:c.1078_1080delinsAGA	XP_006717989.1:p.Asp360Arg
XM_011539982.1:c.1027_1029delinsAGA	XP_011538284.1:p.Asp343Arg
XR_945791.1:n.1693_1695delinsAGA
NM_000314.7:c.1123_1125delinsAGA	NP_000305.3:p.Asp375Arg
NM_001304717.5:c.1642_1644delinsAGA	NP_001291646.4:p.Asp548Arg
NM_001304718.2:c.532_534delinsAGA	NP_001291647.1:p.Asp178Arg
NM_000314.8:c.1123_1125delinsAGA MANE Select	NP_000305.3:p.Asp375Arg