Canonical Allele Identifier: CA891838773

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952151_87952153delinsAGA , CM000672.2:g.87952151_87952153delinsAGA	GRCh38
NC_000010.10:g.89711908_89711910delinsAGA , CM000672.1:g.89711908_89711910delinsAGA	GRCh37
NC_000010.9:g.89701888_89701890delinsAGA	NCBI36
NG_007466.2:g.93713_93715delinsAGA , LRG_311:g.93713_93715delinsAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.526_528delinsAGA	ENSP00000514759.2:p.Tyr176Arg
ENST00000710265.1:c.526_528delinsAGA	ENSP00000518161.1:p.Tyr176Arg
ENST00000472832.3:c.526_528delinsAGA	ENSP00000483066.2:p.Tyr176Arg
ENST00000688158.2:n.1261_1263delinsAGA
ENST00000688922.2:c.*356_*358delinsAGA	ENSP00000508742.2:n.*356_*358delinsAGA
ENST00000700021.1:c.481_483delinsAGA	ENSP00000514757.1:p.Tyr161Arg
ENST00000700022.1:c.493-5702_493-5700delinsAGA	ENSP00000514758.1:n.493-5702_493-5700delinsAGA
ENST00000700023.1:n.1684_1686delinsAGA
ENST00000700024.1:n.1918_1920delinsAGA
ENST00000700025.1:n.1295_1297delinsAGA
ENST00000700029.1:c.360_362delinsAGA
ENST00000706954.1:c.526_528delinsAGA	ENSP00000516674.1:p.Tyr176Arg
ENST00000706955.1:c.*561_*563delinsAGA	ENSP00000516675.1:n.*561_*563delinsAGA
ENST00000686459.1:c.*112_*114delinsAGA	ENSP00000508909.1:n.*112_*114delinsAGA
ENST00000688158.1:c.*637_*639delinsAGA	ENSP00000509254.1:n.*637_*639delinsAGA
ENST00000688308.1:c.526_528delinsAGA	ENSP00000508752.1:p.Tyr176Arg
ENST00000688922.1:c.447_449delinsAGA
ENST00000693560.1:c.1045_1047delinsAGA	ENSP00000509861.1:p.Tyr349Arg
ENST00000371953.8:c.526_528delinsAGA MANE Select	ENSP00000361021.3:p.Tyr176Arg
ENST00000371953.7:c.526_528delinsAGA	ENSP00000361021.3:p.Tyr176Arg
NM_000314.5:c.526_528delinsAGA	NP_000305.3:p.Tyr176Arg
NM_000314.6:c.526_528delinsAGA	NP_000305.3:p.Tyr176Arg
NM_001304717.2:c.1045_1047delinsAGA	NP_001291646.2:p.Tyr349Arg
NM_001304718.1:c.-66_-64delinsAGA	NP_001291647.1:n.-66_-64delinsAGA
XM_006717926.2:c.481_483delinsAGA	XP_006717989.1:p.Tyr161Arg
XM_011539981.1:c.526_528delinsAGA	XP_011538283.1:p.Tyr176Arg
XM_011539982.1:c.430_432delinsAGA	XP_011538284.1:p.Tyr144Arg
XR_945789.1:n.1397_1399delinsAGA
XR_945790.1:n.1514_1516delinsAGA
XR_945791.1:n.1205-5702_1205-5700delinsAGA
NM_000314.7:c.526_528delinsAGA	NP_000305.3:p.Tyr176Arg
NM_001304717.5:c.1045_1047delinsAGA	NP_001291646.4:p.Tyr349Arg
NM_001304718.2:c.-66_-64delinsAGA	NP_001291647.1:n.-66_-64delinsAGA
NM_000314.8:c.526_528delinsAGA MANE Select	NP_000305.3:p.Tyr176Arg