Canonical Allele Identifier: CA891839630

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957918_87957920delinsTAA , CM000672.2:g.87957918_87957920delinsTAA	GRCh38
NC_000010.10:g.89717675_89717677delinsTAA , CM000672.1:g.89717675_89717677delinsTAA	GRCh37
NC_000010.9:g.89707655_89707657delinsTAA	NCBI36
NG_007466.2:g.99480_99482delinsTAA , LRG_311:g.99480_99482delinsTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.700_702delinsTAA	ENSP00000514759.2:p.Arg234Ter
ENST00000710265.1:c.700_702delinsTAA	ENSP00000518161.1:p.Arg234Ter
ENST00000472832.3:c.700_702delinsTAA	ENSP00000483066.2:p.Arg234Ter
ENST00000688158.2:n.1435_1437delinsTAA
ENST00000688922.2:c.*530_*532delinsTAA	ENSP00000508742.2:n.*530_*532delinsTAA
ENST00000700021.1:c.655_657delinsTAA	ENSP00000514757.1:p.Arg219Ter
ENST00000700022.1:c.*39_*41delinsTAA	ENSP00000514758.1:n.*39_*41delinsTAA
ENST00000700023.1:n.1858_1860delinsTAA
ENST00000700024.1:n.2092_2094delinsTAA
ENST00000700025.1:n.1469_1471delinsTAA
ENST00000700026.1:n.337_339delinsTAA
ENST00000700029.1:c.534_536delinsTAA
ENST00000706954.1:c.700_702delinsTAA	ENSP00000516674.1:p.Arg234Ter
ENST00000706955.1:c.*735_*737delinsTAA	ENSP00000516675.1:n.*735_*737delinsTAA
ENST00000686459.1:c.*286_*288delinsTAA	ENSP00000508909.1:n.*286_*288delinsTAA
ENST00000688158.1:c.*811_*813delinsTAA	ENSP00000509254.1:n.*811_*813delinsTAA
ENST00000688308.1:c.700_702delinsTAA	ENSP00000508752.1:p.Arg234Ter
ENST00000688922.1:c.621_623delinsTAA
ENST00000693560.1:c.1219_1221delinsTAA	ENSP00000509861.1:p.Arg407Ter
ENST00000371953.8:c.700_702delinsTAA MANE Select	ENSP00000361021.3:p.Arg234Ter
ENST00000371953.7:c.700_702delinsTAA	ENSP00000361021.3:p.Arg234Ter
ENST00000472832.2:c.127_129delinsTAA	ENSP00000483066.1:p.Arg43Ter
NM_000314.5:c.700_702delinsTAA	NP_000305.3:p.Arg234Ter
NM_000314.6:c.700_702delinsTAA	NP_000305.3:p.Arg234Ter
NM_001304717.2:c.1219_1221delinsTAA	NP_001291646.2:p.Arg407Ter
NM_001304718.1:c.109_111delinsTAA	NP_001291647.1:p.Arg37Ter
XM_006717926.2:c.655_657delinsTAA	XP_006717989.1:p.Arg219Ter
XM_011539981.1:c.700_702delinsTAA	XP_011538283.1:p.Arg234Ter
XM_011539982.1:c.604_606delinsTAA	XP_011538284.1:p.Arg202Ter
XR_945791.1:n.1270_1272delinsTAA
NM_000314.7:c.700_702delinsTAA	NP_000305.3:p.Arg234Ter
NM_001304717.5:c.1219_1221delinsTAA	NP_001291646.4:p.Arg407Ter
NM_001304718.2:c.109_111delinsTAA	NP_001291647.1:p.Arg37Ter
NM_000314.8:c.700_702delinsTAA MANE Select	NP_000305.3:p.Arg234Ter