Canonical Allele Identifier: CA891835187

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960958_87960959delinsTT , CM000672.2:g.87960958_87960959delinsTT	GRCh38
NC_000010.10:g.89720715_89720716delinsTT , CM000672.1:g.89720715_89720716delinsTT	GRCh37
NC_000010.9:g.89710695_89710696delinsTT	NCBI36
NG_007466.2:g.102520_102521delinsTT , LRG_311:g.102520_102521delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.959_960delinsTT	ENSP00000514759.2:p.Lys320Ile
ENST00000710265.1:c.866_867delinsTT	ENSP00000518161.1:p.Lys289Ile
ENST00000472832.3:c.866_867delinsTT	ENSP00000483066.2:p.Lys289Ile
ENST00000688158.2:n.1601_1602delinsTT
ENST00000688922.2:c.*696_*697delinsTT	ENSP00000508742.2:n.*696_*697delinsTT
ENST00000700021.1:c.821_822delinsTT	ENSP00000514757.1:p.Lys274Ile
ENST00000700022.1:c.*205_*206delinsTT	ENSP00000514758.1:n.*205_*206delinsTT
ENST00000700023.1:n.2024_2025delinsTT
ENST00000700024.1:n.2258_2259delinsTT
ENST00000700025.1:n.1635_1636delinsTT
ENST00000700026.1:n.503_504delinsTT
ENST00000700029.1:c.793_794delinsTT
ENST00000706954.1:c.866_867delinsTT	ENSP00000516674.1:p.Lys289Ile
ENST00000706955.1:c.*901_*902delinsTT	ENSP00000516675.1:n.*901_*902delinsTT
ENST00000686459.1:c.*452_*453delinsTT	ENSP00000508909.1:n.*452_*453delinsTT
ENST00000688158.1:c.*977_*978delinsTT	ENSP00000509254.1:n.*977_*978delinsTT
ENST00000688308.1:c.866_867delinsTT	ENSP00000508752.1:p.Lys289Ile
ENST00000688922.1:c.787_788delinsTT
ENST00000693560.1:c.1385_1386delinsTT	ENSP00000509861.1:p.Lys462Ile
ENST00000371953.8:c.866_867delinsTT MANE Select	ENSP00000361021.3:p.Lys289Ile
ENST00000371953.7:c.866_867delinsTT	ENSP00000361021.3:p.Lys289Ile
ENST00000472832.2:c.293_294delinsTT	ENSP00000483066.1:p.Lys98Ile
NM_000314.5:c.866_867delinsTT	NP_000305.3:p.Lys289Ile
NM_000314.6:c.866_867delinsTT	NP_000305.3:p.Lys289Ile
NM_001304717.2:c.1385_1386delinsTT	NP_001291646.2:p.Lys462Ile
NM_001304718.1:c.275_276delinsTT	NP_001291647.1:p.Lys92Ile
XM_006717926.2:c.821_822delinsTT	XP_006717989.1:p.Lys274Ile
XM_011539981.1:c.866_867delinsTT	XP_011538283.1:p.Lys289Ile
XM_011539982.1:c.770_771delinsTT	XP_011538284.1:p.Lys257Ile
XR_945791.1:n.1436_1437delinsTT
NM_000314.7:c.866_867delinsTT	NP_000305.3:p.Lys289Ile
NM_001304717.5:c.1385_1386delinsTT	NP_001291646.4:p.Lys462Ile
NM_001304718.2:c.275_276delinsTT	NP_001291647.1:p.Lys92Ile
NM_000314.8:c.866_867delinsTT MANE Select	NP_000305.3:p.Lys289Ile