Canonical Allele Identifier: CA891835167

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960957_87960959delinsTGT , CM000672.2:g.87960957_87960959delinsTGT	GRCh38
NC_000010.10:g.89720714_89720716delinsTGT , CM000672.1:g.89720714_89720716delinsTGT	GRCh37
NC_000010.9:g.89710694_89710696delinsTGT	NCBI36
NG_007466.2:g.102519_102521delinsTGT , LRG_311:g.102519_102521delinsTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.958_960delinsTGT	ENSP00000514759.2:p.Lys320Cys
ENST00000710265.1:c.865_867delinsTGT	ENSP00000518161.1:p.Lys289Cys
ENST00000472832.3:c.865_867delinsTGT	ENSP00000483066.2:p.Lys289Cys
ENST00000688158.2:n.1600_1602delinsTGT
ENST00000688922.2:c.*695_*697delinsTGT	ENSP00000508742.2:n.*695_*697delinsTGT
ENST00000700021.1:c.820_822delinsTGT	ENSP00000514757.1:p.Lys274Cys
ENST00000700022.1:c.*204_*206delinsTGT	ENSP00000514758.1:n.*204_*206delinsTGT
ENST00000700023.1:n.2023_2025delinsTGT
ENST00000700024.1:n.2257_2259delinsTGT
ENST00000700025.1:n.1634_1636delinsTGT
ENST00000700026.1:n.502_504delinsTGT
ENST00000700029.1:c.792_794delinsTGT
ENST00000706954.1:c.865_867delinsTGT	ENSP00000516674.1:p.Lys289Cys
ENST00000706955.1:c.*900_*902delinsTGT	ENSP00000516675.1:n.*900_*902delinsTGT
ENST00000686459.1:c.*451_*453delinsTGT	ENSP00000508909.1:n.*451_*453delinsTGT
ENST00000688158.1:c.*976_*978delinsTGT	ENSP00000509254.1:n.*976_*978delinsTGT
ENST00000688308.1:c.865_867delinsTGT	ENSP00000508752.1:p.Lys289Cys
ENST00000688922.1:c.786_788delinsTGT
ENST00000693560.1:c.1384_1386delinsTGT	ENSP00000509861.1:p.Lys462Cys
ENST00000371953.8:c.865_867delinsTGT MANE Select	ENSP00000361021.3:p.Lys289Cys
ENST00000371953.7:c.865_867delinsTGT	ENSP00000361021.3:p.Lys289Cys
ENST00000472832.2:c.292_294delinsTGT	ENSP00000483066.1:p.Lys98Cys
NM_000314.5:c.865_867delinsTGT	NP_000305.3:p.Lys289Cys
NM_000314.6:c.865_867delinsTGT	NP_000305.3:p.Lys289Cys
NM_001304717.2:c.1384_1386delinsTGT	NP_001291646.2:p.Lys462Cys
NM_001304718.1:c.274_276delinsTGT	NP_001291647.1:p.Lys92Cys
XM_006717926.2:c.820_822delinsTGT	XP_006717989.1:p.Lys274Cys
XM_011539981.1:c.865_867delinsTGT	XP_011538283.1:p.Lys289Cys
XM_011539982.1:c.769_771delinsTGT	XP_011538284.1:p.Lys257Cys
XR_945791.1:n.1435_1437delinsTGT
NM_000314.7:c.865_867delinsTGT	NP_000305.3:p.Lys289Cys
NM_001304717.5:c.1384_1386delinsTGT	NP_001291646.4:p.Lys462Cys
NM_001304718.2:c.274_276delinsTGT	NP_001291647.1:p.Lys92Cys
NM_000314.8:c.865_867delinsTGT MANE Select	NP_000305.3:p.Lys289Cys