Canonical Allele Identifier: CA891835171

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960957_87960959delinsTAT , CM000672.2:g.87960957_87960959delinsTAT	GRCh38
NC_000010.10:g.89720714_89720716delinsTAT , CM000672.1:g.89720714_89720716delinsTAT	GRCh37
NC_000010.9:g.89710694_89710696delinsTAT	NCBI36
NG_007466.2:g.102519_102521delinsTAT , LRG_311:g.102519_102521delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.958_960delinsTAT	ENSP00000514759.2:p.Lys320Tyr
ENST00000710265.1:c.865_867delinsTAT	ENSP00000518161.1:p.Lys289Tyr
ENST00000472832.3:c.865_867delinsTAT	ENSP00000483066.2:p.Lys289Tyr
ENST00000688158.2:n.1600_1602delinsTAT
ENST00000688922.2:c.*695_*697delinsTAT	ENSP00000508742.2:n.*695_*697delinsTAT
ENST00000700021.1:c.820_822delinsTAT	ENSP00000514757.1:p.Lys274Tyr
ENST00000700022.1:c.*204_*206delinsTAT	ENSP00000514758.1:n.*204_*206delinsTAT
ENST00000700023.1:n.2023_2025delinsTAT
ENST00000700024.1:n.2257_2259delinsTAT
ENST00000700025.1:n.1634_1636delinsTAT
ENST00000700026.1:n.502_504delinsTAT
ENST00000700029.1:c.792_794delinsTAT
ENST00000706954.1:c.865_867delinsTAT	ENSP00000516674.1:p.Lys289Tyr
ENST00000706955.1:c.*900_*902delinsTAT	ENSP00000516675.1:n.*900_*902delinsTAT
ENST00000686459.1:c.*451_*453delinsTAT	ENSP00000508909.1:n.*451_*453delinsTAT
ENST00000688158.1:c.*976_*978delinsTAT	ENSP00000509254.1:n.*976_*978delinsTAT
ENST00000688308.1:c.865_867delinsTAT	ENSP00000508752.1:p.Lys289Tyr
ENST00000688922.1:c.786_788delinsTAT
ENST00000693560.1:c.1384_1386delinsTAT	ENSP00000509861.1:p.Lys462Tyr
ENST00000371953.8:c.865_867delinsTAT MANE Select	ENSP00000361021.3:p.Lys289Tyr
ENST00000371953.7:c.865_867delinsTAT	ENSP00000361021.3:p.Lys289Tyr
ENST00000472832.2:c.292_294delinsTAT	ENSP00000483066.1:p.Lys98Tyr
NM_000314.5:c.865_867delinsTAT	NP_000305.3:p.Lys289Tyr
NM_000314.6:c.865_867delinsTAT	NP_000305.3:p.Lys289Tyr
NM_001304717.2:c.1384_1386delinsTAT	NP_001291646.2:p.Lys462Tyr
NM_001304718.1:c.274_276delinsTAT	NP_001291647.1:p.Lys92Tyr
XM_006717926.2:c.820_822delinsTAT	XP_006717989.1:p.Lys274Tyr
XM_011539981.1:c.865_867delinsTAT	XP_011538283.1:p.Lys289Tyr
XM_011539982.1:c.769_771delinsTAT	XP_011538284.1:p.Lys257Tyr
XR_945791.1:n.1435_1437delinsTAT
NM_000314.7:c.865_867delinsTAT	NP_000305.3:p.Lys289Tyr
NM_001304717.5:c.1384_1386delinsTAT	NP_001291646.4:p.Lys462Tyr
NM_001304718.2:c.274_276delinsTAT	NP_001291647.1:p.Lys92Tyr
NM_000314.8:c.865_867delinsTAT MANE Select	NP_000305.3:p.Lys289Tyr