Canonical Allele Identifier: CA891838134

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933180_87933182delinsTTG , CM000672.2:g.87933180_87933182delinsTTG	GRCh38
NC_000010.10:g.89692937_89692939delinsTTG , CM000672.1:g.89692937_89692939delinsTTG	GRCh37
NC_000010.9:g.89682917_89682919delinsTTG	NCBI36
NG_007466.2:g.74742_74744delinsTTG , LRG_311:g.74742_74744delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
NM_000314.8:c.421_423delinsTTG MANE Select	NP_000305.3:p.His141Leu
ENST00000371953.8:c.421_423delinsTTG MANE Select	ENSP00000361021.3:p.His141Leu
NM_000314.5:c.421_423delinsTTG	NP_000305.3:p.His141Leu
NM_000314.6:c.421_423delinsTTG	NP_000305.3:p.His141Leu
NM_000314.7:c.421_423delinsTTG	NP_000305.3:p.His141Leu
NM_001304717.2:c.940_942delinsTTG	NP_001291646.2:p.His314Leu
NM_001304717.5:c.940_942delinsTTG	NP_001291646.4:p.His314Leu
NM_001304718.1:c.-330_-328delinsTTG	NP_001291647.1:n.-330_-328delinsTTG
NM_001304718.2:c.-330_-328delinsTTG	NP_001291647.1:n.-330_-328delinsTTG
ENST00000371953.7:c.421_423delinsTTG	ENSP00000361021.3:p.His141Leu
ENST00000472832.3:c.421_423delinsTTG	ENSP00000483066.2:p.His141Leu
ENST00000498703.1:n.247_249delinsTTG
ENST00000610634.1:c.319_321delinsTTG	ENSP00000477517.1:p.His107Leu
ENST00000686459.1:c.421_423delinsTTG	ENSP00000508909.1:p.His141Leu
ENST00000688158.1:c.*532_*534delinsTTG	ENSP00000509254.1:n.*532_*534delinsTTG
ENST00000688158.2:n.1156_1158delinsTTG
ENST00000688308.1:c.421_423delinsTTG	ENSP00000508752.1:p.His141Leu
ENST00000688922.1:c.342_344delinsTTG
ENST00000688922.2:c.*251_*253delinsTTG	ENSP00000508742.2:n.*251_*253delinsTTG
ENST00000693560.1:c.940_942delinsTTG	ENSP00000509861.1:p.His314Leu
ENST00000700021.1:c.376_378delinsTTG	ENSP00000514757.1:p.His126Leu
ENST00000700022.1:c.421_423delinsTTG	ENSP00000514758.1:p.His141Leu
ENST00000700029.1:c.255_257delinsTTG
ENST00000700029.2:c.421_423delinsTTG	ENSP00000514759.2:p.His141Leu
ENST00000706954.1:c.421_423delinsTTG	ENSP00000516674.1:p.His141Leu
ENST00000706955.1:c.*456_*458delinsTTG	ENSP00000516675.1:n.*456_*458delinsTTG
ENST00000710265.1:c.421_423delinsTTG	ENSP00000518161.1:p.His141Leu
XM_006717926.2:c.376_378delinsTTG	XP_006717989.1:p.His126Leu
XM_011539981.1:c.421_423delinsTTG	XP_011538283.1:p.His141Leu
XM_011539982.1:c.325_327delinsTTG	XP_011538284.1:p.His109Leu
XR_945789.1:n.1133_1135delinsTTG
XR_945790.1:n.1133_1135delinsTTG
XR_945791.1:n.1133_1135delinsTTG