Canonical Allele Identifier: CA891841485

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965290_87965291delinsTG , CM000672.2:g.87965290_87965291delinsTG	GRCh38
NC_000010.10:g.89725047_89725048delinsTG , CM000672.1:g.89725047_89725048delinsTG	GRCh37
NC_000010.9:g.89715027_89715028delinsTG	NCBI36
NG_007466.2:g.106852_106853delinsTG , LRG_311:g.106852_106853delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1123_1124delinsTG	ENSP00000514759.2:p.Lys375Trp
ENST00000710265.1:c.*59_*60delinsTG	ENSP00000518161.1:n.*59_*60delinsTG
ENST00000688158.2:n.1765_1766delinsTG
ENST00000688922.2:c.*860_*861delinsTG	ENSP00000508742.2:n.*860_*861delinsTG
ENST00000700021.1:c.985_986delinsTG	ENSP00000514757.1:p.Lys329Trp
ENST00000700022.1:c.*369_*370delinsTG	ENSP00000514758.1:n.*369_*370delinsTG
ENST00000700023.1:n.2188_2189delinsTG
ENST00000700024.1:n.2422_2423delinsTG
ENST00000706954.1:c.1030_1031delinsTG	ENSP00000516674.1:p.Lys344Trp
ENST00000706955.1:c.*1065_*1066delinsTG	ENSP00000516675.1:n.*1065_*1066delinsTG
ENST00000686459.1:c.*616_*617delinsTG	ENSP00000508909.1:n.*616_*617delinsTG
ENST00000688158.1:c.*1141_*1142delinsTG	ENSP00000509254.1:n.*1141_*1142delinsTG
ENST00000688308.1:c.1030_1031delinsTG	ENSP00000508752.1:p.Lys344Trp
ENST00000688922.1:c.951_952delinsTG
ENST00000693560.1:c.1549_1550delinsTG	ENSP00000509861.1:p.Lys517Trp
ENST00000371953.8:c.1030_1031delinsTG MANE Select	ENSP00000361021.3:p.Lys344Trp
ENST00000371953.7:c.1030_1031delinsTG	ENSP00000361021.3:p.Lys344Trp
NM_000314.5:c.1030_1031delinsTG	NP_000305.3:p.Lys344Trp
NM_000314.6:c.1030_1031delinsTG	NP_000305.3:p.Lys344Trp
NM_001304717.2:c.1549_1550delinsTG	NP_001291646.2:p.Lys517Trp
NM_001304718.1:c.439_440delinsTG	NP_001291647.1:p.Lys147Trp
XM_006717926.2:c.985_986delinsTG	XP_006717989.1:p.Lys329Trp
XM_011539982.1:c.934_935delinsTG	XP_011538284.1:p.Lys312Trp
XR_945791.1:n.1600_1601delinsTG
NM_000314.7:c.1030_1031delinsTG	NP_000305.3:p.Lys344Trp
NM_001304717.5:c.1549_1550delinsTG	NP_001291646.4:p.Lys517Trp
NM_001304718.2:c.439_440delinsTG	NP_001291647.1:p.Lys147Trp
NM_000314.8:c.1030_1031delinsTG MANE Select	NP_000305.3:p.Lys344Trp