Canonical Allele Identifier: CA891841396

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961093_87961094delinsTG , CM000672.2:g.87961093_87961094delinsTG	GRCh38
NC_000010.10:g.89720850_89720851delinsTG , CM000672.1:g.89720850_89720851delinsTG	GRCh37
NC_000010.9:g.89710830_89710831delinsTG	NCBI36
NG_007466.2:g.102655_102656delinsTG , LRG_311:g.102655_102656delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1094_1095delinsTG	ENSP00000514759.2:p.Asn365Met
ENST00000710265.1:c.1001_1002delinsTG	ENSP00000518161.1:p.Asn334Met
ENST00000472832.3:c.1001_1002delinsTG	ENSP00000483066.2:p.Asn334Met
ENST00000688158.2:n.1736_1737delinsTG
ENST00000688922.2:c.*831_*832delinsTG	ENSP00000508742.2:n.*831_*832delinsTG
ENST00000700021.1:c.956_957delinsTG	ENSP00000514757.1:p.Asn319Met
ENST00000700022.1:c.*340_*341delinsTG	ENSP00000514758.1:n.*340_*341delinsTG
ENST00000700023.1:n.2159_2160delinsTG
ENST00000700024.1:n.2393_2394delinsTG
ENST00000700025.1:n.1770_1771delinsTG
ENST00000700026.1:n.638_639delinsTG
ENST00000706954.1:c.1001_1002delinsTG	ENSP00000516674.1:p.Asn334Met
ENST00000706955.1:c.*1036_*1037delinsTG	ENSP00000516675.1:n.*1036_*1037delinsTG
ENST00000686459.1:c.*587_*588delinsTG	ENSP00000508909.1:n.*587_*588delinsTG
ENST00000688158.1:c.*1112_*1113delinsTG	ENSP00000509254.1:n.*1112_*1113delinsTG
ENST00000688308.1:c.1001_1002delinsTG	ENSP00000508752.1:p.Asn334Met
ENST00000688922.1:c.922_923delinsTG
ENST00000693560.1:c.1520_1521delinsTG	ENSP00000509861.1:p.Asn507Met
ENST00000371953.8:c.1001_1002delinsTG MANE Select	ENSP00000361021.3:p.Asn334Met
ENST00000371953.7:c.1001_1002delinsTG	ENSP00000361021.3:p.Asn334Met
ENST00000472832.2:c.428_429delinsTG	ENSP00000483066.1:p.Asn143Met
NM_000314.5:c.1001_1002delinsTG	NP_000305.3:p.Asn334Met
NM_000314.6:c.1001_1002delinsTG	NP_000305.3:p.Asn334Met
NM_001304717.2:c.1520_1521delinsTG	NP_001291646.2:p.Asn507Met
NM_001304718.1:c.410_411delinsTG	NP_001291647.1:p.Asn137Met
XM_006717926.2:c.956_957delinsTG	XP_006717989.1:p.Asn319Met
XM_011539981.1:c.1001_1002delinsTG	XP_011538283.1:p.Asn334Met
XM_011539982.1:c.905_906delinsTG	XP_011538284.1:p.Asn302Met
XR_945791.1:n.1571_1572delinsTG
NM_000314.7:c.1001_1002delinsTG	NP_000305.3:p.Asn334Met
NM_001304717.5:c.1520_1521delinsTG	NP_001291646.4:p.Asn507Met
NM_001304718.2:c.410_411delinsTG	NP_001291647.1:p.Asn137Met
NM_000314.8:c.1001_1002delinsTG MANE Select	NP_000305.3:p.Asn334Met