Canonical Allele Identifier: CA891839067

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952211_87952213delinsAGA , CM000672.2:g.87952211_87952213delinsAGA	GRCh38
NC_000010.10:g.89711968_89711970delinsAGA , CM000672.1:g.89711968_89711970delinsAGA	GRCh37
NC_000010.9:g.89701948_89701950delinsAGA	NCBI36
NG_007466.2:g.93773_93775delinsAGA , LRG_311:g.93773_93775delinsAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.586_588delinsAGA	ENSP00000514759.2:p.His196Arg
ENST00000710265.1:c.586_588delinsAGA	ENSP00000518161.1:p.His196Arg
ENST00000472832.3:c.586_588delinsAGA	ENSP00000483066.2:p.His196Arg
ENST00000688158.2:n.1321_1323delinsAGA
ENST00000688922.2:c.*416_*418delinsAGA	ENSP00000508742.2:n.*416_*418delinsAGA
ENST00000700021.1:c.541_543delinsAGA	ENSP00000514757.1:p.His181Arg
ENST00000700022.1:c.493-5642_493-5640delinsAGA	ENSP00000514758.1:n.493-5642_493-5640delinsAGA
ENST00000700023.1:n.1744_1746delinsAGA
ENST00000700024.1:n.1978_1980delinsAGA
ENST00000700025.1:n.1355_1357delinsAGA
ENST00000700029.1:c.420_422delinsAGA
ENST00000706954.1:c.586_588delinsAGA	ENSP00000516674.1:p.His196Arg
ENST00000706955.1:c.*621_*623delinsAGA	ENSP00000516675.1:n.*621_*623delinsAGA
ENST00000686459.1:c.*172_*174delinsAGA	ENSP00000508909.1:n.*172_*174delinsAGA
ENST00000688158.1:c.*697_*699delinsAGA	ENSP00000509254.1:n.*697_*699delinsAGA
ENST00000688308.1:c.586_588delinsAGA	ENSP00000508752.1:p.His196Arg
ENST00000688922.1:c.507_509delinsAGA
ENST00000693560.1:c.1105_1107delinsAGA	ENSP00000509861.1:p.His369Arg
ENST00000371953.8:c.586_588delinsAGA MANE Select	ENSP00000361021.3:p.His196Arg
ENST00000371953.7:c.586_588delinsAGA	ENSP00000361021.3:p.His196Arg
ENST00000472832.2:c.13_15delinsAGA	ENSP00000483066.1:p.His5Arg
NM_000314.5:c.586_588delinsAGA	NP_000305.3:p.His196Arg
NM_000314.6:c.586_588delinsAGA	NP_000305.3:p.His196Arg
NM_001304717.2:c.1105_1107delinsAGA	NP_001291646.2:p.His369Arg
NM_001304718.1:c.-6_-4delinsAGA	NP_001291647.1:n.-6_-4delinsAGA
XM_006717926.2:c.541_543delinsAGA	XP_006717989.1:p.His181Arg
XM_011539981.1:c.586_588delinsAGA	XP_011538283.1:p.His196Arg
XM_011539982.1:c.490_492delinsAGA	XP_011538284.1:p.His164Arg
XR_945791.1:n.1205-5642_1205-5640delinsAGA
NM_000314.7:c.586_588delinsAGA	NP_000305.3:p.His196Arg
NM_001304717.5:c.1105_1107delinsAGA	NP_001291646.4:p.His369Arg
NM_001304718.2:c.-6_-4delinsAGA	NP_001291647.1:n.-6_-4delinsAGA
NM_000314.8:c.586_588delinsAGA MANE Select	NP_000305.3:p.His196Arg