Canonical Allele Identifier: CA2579926811

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957918_87957920del , CM000672.2:g.87957918_87957920del	GRCh38
NC_000010.10:g.89717675_89717677del , CM000672.1:g.89717675_89717677del	GRCh37
NC_000010.9:g.89707655_89707657del	NCBI36
NG_007466.2:g.99480_99482del , LRG_311:g.99480_99482del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.700_702del	ENSP00000514759.2:p.Arg234del
ENST00000710265.1:c.700_702del	ENSP00000518161.1:p.Arg234del
ENST00000472832.3:c.700_702del	ENSP00000483066.2:p.Arg234del
ENST00000688158.2:n.1435_1437del
ENST00000688922.2:c.*530_*532del	ENSP00000508742.2:n.*530_*532del
ENST00000700021.1:c.655_657del	ENSP00000514757.1:p.Arg219del
ENST00000700022.1:c.*39_*41del	ENSP00000514758.1:n.*39_*41del
ENST00000700023.1:n.1858_1860del
ENST00000700024.1:n.2092_2094del
ENST00000700025.1:n.1469_1471del
ENST00000700026.1:n.337_339del
ENST00000700029.1:c.534_536del
ENST00000706954.1:c.700_702del	ENSP00000516674.1:p.Arg234del
ENST00000706955.1:c.*735_*737del	ENSP00000516675.1:n.*735_*737del
ENST00000686459.1:c.*286_*288del	ENSP00000508909.1:n.*286_*288del
ENST00000688158.1:c.*811_*813del	ENSP00000509254.1:n.*811_*813del
ENST00000688308.1:c.700_702del	ENSP00000508752.1:p.Arg234del
ENST00000688922.1:c.621_623del
ENST00000693560.1:c.1219_1221del	ENSP00000509861.1:p.Arg407del
ENST00000371953.8:c.700_702del MANE Select	ENSP00000361021.3:p.Arg234del
ENST00000371953.7:c.700_702del	ENSP00000361021.3:p.Arg234del
ENST00000472832.2:c.127_129del	ENSP00000483066.1:p.Arg43del
NM_000314.5:c.700_702del	NP_000305.3:p.Arg234del
NM_000314.6:c.700_702del	NP_000305.3:p.Arg234del
NM_001304717.2:c.1219_1221del	NP_001291646.2:p.Arg407del
NM_001304718.1:c.109_111del	NP_001291647.1:p.Arg37del
XM_006717926.2:c.655_657del	XP_006717989.1:p.Arg219del
XM_011539981.1:c.700_702del	XP_011538283.1:p.Arg234del
XM_011539982.1:c.604_606del	XP_011538284.1:p.Arg202del
XR_945791.1:n.1270_1272del
NM_000314.7:c.700_702del	NP_000305.3:p.Arg234del
NM_001304717.5:c.1219_1221del	NP_001291646.4:p.Arg407del
NM_001304718.2:c.109_111del	NP_001291647.1:p.Arg37del
NM_000314.8:c.700_702del MANE Select	NP_000305.3:p.Arg234del