Canonical Allele Identifier: CA891838798

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952157_87952159delinsAGA , CM000672.2:g.87952157_87952159delinsAGA	GRCh38
NC_000010.10:g.89711914_89711916delinsAGA , CM000672.1:g.89711914_89711916delinsAGA	GRCh37
NC_000010.9:g.89701894_89701896delinsAGA	NCBI36
NG_007466.2:g.93719_93721delinsAGA , LRG_311:g.93719_93721delinsAGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.532_534delinsAGA	ENSP00000514759.2:p.Tyr178Arg
ENST00000710265.1:c.532_534delinsAGA	ENSP00000518161.1:p.Tyr178Arg
ENST00000472832.3:c.532_534delinsAGA	ENSP00000483066.2:p.Tyr178Arg
ENST00000688158.2:n.1267_1269delinsAGA
ENST00000688922.2:c.*362_*364delinsAGA	ENSP00000508742.2:n.*362_*364delinsAGA
ENST00000700021.1:c.487_489delinsAGA	ENSP00000514757.1:p.Tyr163Arg
ENST00000700022.1:c.493-5696_493-5694delinsAGA	ENSP00000514758.1:n.493-5696_493-5694deli...
ENST00000700023.1:n.1690_1692delinsAGA
ENST00000700024.1:n.1924_1926delinsAGA
ENST00000700025.1:n.1301_1303delinsAGA
ENST00000700029.1:c.366_368delinsAGA
ENST00000706954.1:c.532_534delinsAGA	ENSP00000516674.1:p.Tyr178Arg
ENST00000706955.1:c.*567_*569delinsAGA	ENSP00000516675.1:n.*567_*569delinsAGA
ENST00000686459.1:c.*118_*120delinsAGA	ENSP00000508909.1:n.*118_*120delinsAGA
ENST00000688158.1:c.*643_*645delinsAGA	ENSP00000509254.1:n.*643_*645delinsAGA
ENST00000688308.1:c.532_534delinsAGA	ENSP00000508752.1:p.Tyr178Arg
ENST00000688922.1:c.453_455delinsAGA
ENST00000693560.1:c.1051_1053delinsAGA	ENSP00000509861.1:p.Tyr351Arg
ENST00000371953.8:c.532_534delinsAGA MANE Select	ENSP00000361021.3:p.Tyr178Arg
ENST00000371953.7:c.532_534delinsAGA	ENSP00000361021.3:p.Tyr178Arg
NM_000314.5:c.532_534delinsAGA	NP_000305.3:p.Tyr178Arg
NM_000314.6:c.532_534delinsAGA	NP_000305.3:p.Tyr178Arg
NM_001304717.2:c.1051_1053delinsAGA	NP_001291646.2:p.Tyr351Arg
NM_001304718.1:c.-60_-58delinsAGA	NP_001291647.1:n.-60_-58delinsAGA
XM_006717926.2:c.487_489delinsAGA	XP_006717989.1:p.Tyr163Arg
XM_011539981.1:c.532_534delinsAGA	XP_011538283.1:p.Tyr178Arg
XM_011539982.1:c.436_438delinsAGA	XP_011538284.1:p.Tyr146Arg
XR_945789.1:n.1403_1405delinsAGA
XR_945790.1:n.1520_1522delinsAGA
XR_945791.1:n.1205-5696_1205-5694delinsAGA
NM_000314.7:c.532_534delinsAGA	NP_000305.3:p.Tyr178Arg
NM_001304717.5:c.1051_1053delinsAGA	NP_001291646.4:p.Tyr351Arg
NM_001304718.2:c.-60_-58delinsAGA	NP_001291647.1:n.-60_-58delinsAGA
NM_000314.8:c.532_534delinsAGA MANE Select	NP_000305.3:p.Tyr178Arg