Canonical Allele Identifier: CA891838803

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952157_87952158delinsGT , CM000672.2:g.87952157_87952158delinsGT	GRCh38
NC_000010.10:g.89711914_89711915delinsGT , CM000672.1:g.89711914_89711915delinsGT	GRCh37
NC_000010.9:g.89701894_89701895delinsGT	NCBI36
NG_007466.2:g.93719_93720delinsGT , LRG_311:g.93719_93720delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.532_533delinsGT	ENSP00000514759.2:p.Tyr178Val
ENST00000710265.1:c.532_533delinsGT	ENSP00000518161.1:p.Tyr178Val
ENST00000472832.3:c.532_533delinsGT	ENSP00000483066.2:p.Tyr178Val
ENST00000688158.2:n.1267_1268delinsGT
ENST00000688922.2:c.*362_*363delinsGT	ENSP00000508742.2:n.*362_*363delinsGT
ENST00000700021.1:c.487_488delinsGT	ENSP00000514757.1:p.Tyr163Val
ENST00000700022.1:c.493-5696_493-5695delinsGT	ENSP00000514758.1:n.493-5696_493-5695deli...
ENST00000700023.1:n.1690_1691delinsGT
ENST00000700024.1:n.1924_1925delinsGT
ENST00000700025.1:n.1301_1302delinsGT
ENST00000700029.1:c.366_367delinsGT
ENST00000706954.1:c.532_533delinsGT	ENSP00000516674.1:p.Tyr178Val
ENST00000706955.1:c.*567_*568delinsGT	ENSP00000516675.1:n.*567_*568delinsGT
ENST00000686459.1:c.*118_*119delinsGT	ENSP00000508909.1:n.*118_*119delinsGT
ENST00000688158.1:c.*643_*644delinsGT	ENSP00000509254.1:n.*643_*644delinsGT
ENST00000688308.1:c.532_533delinsGT	ENSP00000508752.1:p.Tyr178Val
ENST00000688922.1:c.453_454delinsGT
ENST00000693560.1:c.1051_1052delinsGT	ENSP00000509861.1:p.Tyr351Val
ENST00000371953.8:c.532_533delinsGT MANE Select	ENSP00000361021.3:p.Tyr178Val
ENST00000371953.7:c.532_533delinsGT	ENSP00000361021.3:p.Tyr178Val
NM_000314.5:c.532_533delinsGT	NP_000305.3:p.Tyr178Val
NM_000314.6:c.532_533delinsGT	NP_000305.3:p.Tyr178Val
NM_001304717.2:c.1051_1052delinsGT	NP_001291646.2:p.Tyr351Val
NM_001304718.1:c.-60_-59delinsGT	NP_001291647.1:n.-60_-59delinsGT
XM_006717926.2:c.487_488delinsGT	XP_006717989.1:p.Tyr163Val
XM_011539981.1:c.532_533delinsGT	XP_011538283.1:p.Tyr178Val
XM_011539982.1:c.436_437delinsGT	XP_011538284.1:p.Tyr146Val
XR_945789.1:n.1403_1404delinsGT
XR_945790.1:n.1520_1521delinsGT
XR_945791.1:n.1205-5696_1205-5695delinsGT
NM_000314.7:c.532_533delinsGT	NP_000305.3:p.Tyr178Val
NM_001304717.5:c.1051_1052delinsGT	NP_001291646.4:p.Tyr351Val
NM_001304718.2:c.-60_-59delinsGT	NP_001291647.1:n.-60_-59delinsGT
NM_000314.8:c.532_533delinsGT MANE Select	NP_000305.3:p.Tyr178Val