Canonical Allele Identifier: CA891836586

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961051_87961052delinsCT , CM000672.2:g.87961051_87961052delinsCT	GRCh38
NC_000010.10:g.89720808_89720809delinsCT , CM000672.1:g.89720808_89720809delinsCT	GRCh37
NC_000010.9:g.89710788_89710789delinsCT	NCBI36
NG_007466.2:g.102613_102614delinsCT , LRG_311:g.102613_102614delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1052_1053delinsCT	ENSP00000514759.2:p.Leu351Ser
ENST00000710265.1:c.959_960delinsCT	ENSP00000518161.1:p.Leu320Ser
ENST00000472832.3:c.959_960delinsCT	ENSP00000483066.2:p.Leu320Ser
ENST00000688158.2:n.1694_1695delinsCT
ENST00000688922.2:c.*789_*790delinsCT	ENSP00000508742.2:n.*789_*790delinsCT
ENST00000700021.1:c.914_915delinsCT	ENSP00000514757.1:p.Leu305Ser
ENST00000700022.1:c.*298_*299delinsCT	ENSP00000514758.1:n.*298_*299delinsCT
ENST00000700023.1:n.2117_2118delinsCT
ENST00000700024.1:n.2351_2352delinsCT
ENST00000700025.1:n.1728_1729delinsCT
ENST00000700026.1:n.596_597delinsCT
ENST00000706954.1:c.959_960delinsCT	ENSP00000516674.1:p.Leu320Ser
ENST00000706955.1:c.*994_*995delinsCT	ENSP00000516675.1:n.*994_*995delinsCT
ENST00000686459.1:c.*545_*546delinsCT	ENSP00000508909.1:n.*545_*546delinsCT
ENST00000688158.1:c.*1070_*1071delinsCT	ENSP00000509254.1:n.*1070_*1071delinsCT
ENST00000688308.1:c.959_960delinsCT	ENSP00000508752.1:p.Leu320Ser
ENST00000688922.1:c.880_881delinsCT
ENST00000693560.1:c.1478_1479delinsCT	ENSP00000509861.1:p.Leu493Ser
ENST00000371953.8:c.959_960delinsCT MANE Select	ENSP00000361021.3:p.Leu320Ser
ENST00000371953.7:c.959_960delinsCT	ENSP00000361021.3:p.Leu320Ser
ENST00000472832.2:c.386_387delinsCT	ENSP00000483066.1:p.Leu129Ser
NM_000314.5:c.959_960delinsCT	NP_000305.3:p.Leu320Ser
NM_000314.6:c.959_960delinsCT	NP_000305.3:p.Leu320Ser
NM_001304717.2:c.1478_1479delinsCT	NP_001291646.2:p.Leu493Ser
NM_001304718.1:c.368_369delinsCT	NP_001291647.1:p.Leu123Ser
XM_006717926.2:c.914_915delinsCT	XP_006717989.1:p.Leu305Ser
XM_011539981.1:c.959_960delinsCT	XP_011538283.1:p.Leu320Ser
XM_011539982.1:c.863_864delinsCT	XP_011538284.1:p.Leu288Ser
XR_945791.1:n.1529_1530delinsCT
NM_000314.7:c.959_960delinsCT	NP_000305.3:p.Leu320Ser
NM_001304717.5:c.1478_1479delinsCT	NP_001291646.4:p.Leu493Ser
NM_001304718.2:c.368_369delinsCT	NP_001291647.1:p.Leu123Ser
NM_000314.8:c.959_960delinsCT MANE Select	NP_000305.3:p.Leu320Ser