Canonical Allele Identifier: CA891841623

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965383_87965384delinsCT , CM000672.2:g.87965383_87965384delinsCT	GRCh38
NC_000010.10:g.89725140_89725141delinsCT , CM000672.1:g.89725140_89725141delinsCT	GRCh37
NC_000010.9:g.89715120_89715121delinsCT	NCBI36
NG_007466.2:g.106945_106946delinsCT , LRG_311:g.106945_106946delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1216_1217delinsCT	ENSP00000514759.2:p.Asp406Leu
ENST00000710265.1:c.*152_*153delinsCT	ENSP00000518161.1:n.*152_*153delinsCT
ENST00000688158.2:n.1858_1859delinsCT
ENST00000688922.2:c.*953_*954delinsCT	ENSP00000508742.2:n.*953_*954delinsCT
ENST00000700021.1:c.1078_1079delinsCT	ENSP00000514757.1:p.Asp360Leu
ENST00000700022.1:c.*462_*463delinsCT	ENSP00000514758.1:n.*462_*463delinsCT
ENST00000700023.1:n.2281_2282delinsCT
ENST00000700024.1:n.2515_2516delinsCT
ENST00000706954.1:c.1123_1124delinsCT	ENSP00000516674.1:p.Asp375Leu
ENST00000706955.1:c.*1158_*1159delinsCT	ENSP00000516675.1:n.*1158_*1159delinsCT
ENST00000686459.1:c.*709_*710delinsCT	ENSP00000508909.1:n.*709_*710delinsCT
ENST00000688158.1:c.*1234_*1235delinsCT	ENSP00000509254.1:n.*1234_*1235delinsCT
ENST00000688308.1:c.1123_1124delinsCT	ENSP00000508752.1:p.Asp375Leu
ENST00000688922.1:c.1044_1045delinsCT
ENST00000693560.1:c.1642_1643delinsCT	ENSP00000509861.1:p.Asp548Leu
ENST00000371953.8:c.1123_1124delinsCT MANE Select	ENSP00000361021.3:p.Asp375Leu
ENST00000371953.7:c.1123_1124delinsCT	ENSP00000361021.3:p.Asp375Leu
NM_000314.5:c.1123_1124delinsCT	NP_000305.3:p.Asp375Leu
NM_000314.6:c.1123_1124delinsCT	NP_000305.3:p.Asp375Leu
NM_001304717.2:c.1642_1643delinsCT	NP_001291646.2:p.Asp548Leu
NM_001304718.1:c.532_533delinsCT	NP_001291647.1:p.Asp178Leu
XM_006717926.2:c.1078_1079delinsCT	XP_006717989.1:p.Asp360Leu
XM_011539982.1:c.1027_1028delinsCT	XP_011538284.1:p.Asp343Leu
XR_945791.1:n.1693_1694delinsCT
NM_000314.7:c.1123_1124delinsCT	NP_000305.3:p.Asp375Leu
NM_001304717.5:c.1642_1643delinsCT	NP_001291646.4:p.Asp548Leu
NM_001304718.2:c.532_533delinsCT	NP_001291647.1:p.Asp178Leu
NM_000314.8:c.1123_1124delinsCT MANE Select	NP_000305.3:p.Asp375Leu