Canonical Allele Identifier: CA2579926720

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960961_87960963del , CM000672.2:g.87960961_87960963del	GRCh38
NC_000010.10:g.89720718_89720720del , CM000672.1:g.89720718_89720720del	GRCh37
NC_000010.9:g.89710698_89710700del	NCBI36
NG_007466.2:g.102523_102525del , LRG_311:g.102523_102525del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.962_964del	ENSP00000514759.2:p.Val321del
ENST00000710265.1:c.869_871del	ENSP00000518161.1:p.Val290del
ENST00000472832.3:c.869_871del	ENSP00000483066.2:p.Val290del
ENST00000688158.2:n.1604_1606del
ENST00000688922.2:c.*699_*701del	ENSP00000508742.2:n.*699_*701del
ENST00000700021.1:c.824_826del	ENSP00000514757.1:p.Val275del
ENST00000700022.1:c.*208_*210del	ENSP00000514758.1:n.*208_*210del
ENST00000700023.1:n.2027_2029del
ENST00000700024.1:n.2261_2263del
ENST00000700025.1:n.1638_1640del
ENST00000700026.1:n.506_508del
ENST00000700029.1:c.796_798del
ENST00000706954.1:c.869_871del	ENSP00000516674.1:p.Val290del
ENST00000706955.1:c.*904_*906del	ENSP00000516675.1:n.*904_*906del
ENST00000686459.1:c.*455_*457del	ENSP00000508909.1:n.*455_*457del
ENST00000688158.1:c.*980_*982del	ENSP00000509254.1:n.*980_*982del
ENST00000688308.1:c.869_871del	ENSP00000508752.1:p.Val290del
ENST00000688922.1:c.790_792del
ENST00000693560.1:c.1388_1390del	ENSP00000509861.1:p.Val463del
ENST00000371953.8:c.869_871del MANE Select	ENSP00000361021.3:p.Val290del
ENST00000371953.7:c.869_871del	ENSP00000361021.3:p.Val290del
ENST00000472832.2:c.296_298del	ENSP00000483066.1:p.Val99del
NM_000314.5:c.869_871del	NP_000305.3:p.Val290del
NM_000314.6:c.869_871del	NP_000305.3:p.Val290del
NM_001304717.2:c.1388_1390del	NP_001291646.2:p.Val463del
NM_001304718.1:c.278_280del	NP_001291647.1:p.Val93del
XM_006717926.2:c.824_826del	XP_006717989.1:p.Val275del
XM_011539981.1:c.869_871del	XP_011538283.1:p.Val290del
XM_011539982.1:c.773_775del	XP_011538284.1:p.Val258del
XR_945791.1:n.1439_1441del
NM_000314.7:c.869_871del	NP_000305.3:p.Val290del
NM_001304717.5:c.1388_1390del	NP_001291646.4:p.Val463del
NM_001304718.2:c.278_280del	NP_001291647.1:p.Val93del
NM_000314.8:c.869_871del MANE Select	NP_000305.3:p.Val290del