Canonical Allele Identifier: CA891834541

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894027_87894029delinsTTG , CM000672.2:g.87894027_87894029delinsTTG	GRCh38
NC_000010.10:g.89653784_89653786delinsTTG , CM000672.1:g.89653784_89653786delinsTTG	GRCh37
NC_000010.9:g.89643764_89643766delinsTTG	NCBI36
NG_007466.2:g.35589_35591delinsTTG , LRG_311:g.35589_35591delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.82_84delinsTTG	ENSP00000514759.2:p.Ile28Leu
ENST00000710265.1:c.82_84delinsTTG	ENSP00000518161.1:p.Ile28Leu
ENST00000472832.3:c.82_84delinsTTG	ENSP00000483066.2:p.Ile28Leu
ENST00000688158.2:n.899+13589_899+13591delinsTTG
ENST00000688922.2:c.82_84delinsTTG	ENSP00000508742.2:p.Ile28Leu
ENST00000700021.1:c.82_84delinsTTG	ENSP00000514757.1:p.Ile28Leu
ENST00000700022.1:c.82_84delinsTTG	ENSP00000514758.1:p.Ile28Leu
ENST00000706954.1:c.82_84delinsTTG	ENSP00000516674.1:p.Ile28Leu
ENST00000706955.1:c.*117_*119delinsTTG	ENSP00000516675.1:n.*117_*119delinsTTG
ENST00000686459.1:c.82_84delinsTTG	ENSP00000508909.1:p.Ile28Leu
ENST00000688158.1:c.*275+13589_*275+13591delinsTTG	ENSP00000509254.1:n.*275+13589_*275+13591delinsTTG
ENST00000688308.1:c.82_84delinsTTG	ENSP00000508752.1:p.Ile28Leu
ENST00000693560.1:c.601_603delinsTTG	ENSP00000509861.1:p.Ile201Leu
ENST00000371953.8:c.82_84delinsTTG MANE Select	ENSP00000361021.3:p.Ile28Leu
ENST00000371953.7:c.82_84delinsTTG	ENSP00000361021.3:p.Ile28Leu
ENST00000462694.1:n.84_86delinsTTG
ENST00000610634.1:c.-21_-19delinsTTG	ENSP00000477517.1:n.-21_-19delinsTTG
NM_000314.5:c.82_84delinsTTG	NP_000305.3:p.Ile28Leu
NM_000314.6:c.82_84delinsTTG	NP_000305.3:p.Ile28Leu
NM_001304717.2:c.601_603delinsTTG	NP_001291646.2:p.Ile201Leu
NM_001304718.1:c.-624_-622delinsTTG	NP_001291647.1:n.-624_-622delinsTTG
XM_006717926.2:c.82_84delinsTTG	XP_006717989.1:p.Ile28Leu
XM_011539981.1:c.82_84delinsTTG	XP_011538283.1:p.Ile28Leu
XM_011539982.1:c.68+13589_68+13591delinsTTG	XP_011538284.1:n.68+13589_68+13591delinsTTG
XR_945789.1:n.794_796delinsTTG
XR_945790.1:n.794_796delinsTTG
XR_945791.1:n.794_796delinsTTG
NM_000314.7:c.82_84delinsTTG	NP_000305.3:p.Ile28Leu
NM_001304717.5:c.601_603delinsTTG	NP_001291646.4:p.Ile201Leu
NM_001304718.2:c.-624_-622delinsTTG	NP_001291647.1:n.-624_-622delinsTTG
NM_000314.8:c.82_84delinsTTG MANE Select	NP_000305.3:p.Ile28Leu