Canonical Allele Identifier: CA891841108

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960957_87960958delinsGT , CM000672.2:g.87960957_87960958delinsGT	GRCh38
NC_000010.10:g.89720714_89720715delinsGT , CM000672.1:g.89720714_89720715delinsGT	GRCh37
NC_000010.9:g.89710694_89710695delinsGT	NCBI36
NG_007466.2:g.102519_102520delinsGT , LRG_311:g.102519_102520delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.958_959delinsGT	ENSP00000514759.2:p.Lys320Val
ENST00000710265.1:c.865_866delinsGT	ENSP00000518161.1:p.Lys289Val
ENST00000472832.3:c.865_866delinsGT	ENSP00000483066.2:p.Lys289Val
ENST00000688158.2:n.1600_1601delinsGT
ENST00000688922.2:c.*695_*696delinsGT	ENSP00000508742.2:n.*695_*696delinsGT
ENST00000700021.1:c.820_821delinsGT	ENSP00000514757.1:p.Lys274Val
ENST00000700022.1:c.*204_*205delinsGT	ENSP00000514758.1:n.*204_*205delinsGT
ENST00000700023.1:n.2023_2024delinsGT
ENST00000700024.1:n.2257_2258delinsGT
ENST00000700025.1:n.1634_1635delinsGT
ENST00000700026.1:n.502_503delinsGT
ENST00000700029.1:c.792_793delinsGT
ENST00000706954.1:c.865_866delinsGT	ENSP00000516674.1:p.Lys289Val
ENST00000706955.1:c.*900_*901delinsGT	ENSP00000516675.1:n.*900_*901delinsGT
ENST00000686459.1:c.*451_*452delinsGT	ENSP00000508909.1:n.*451_*452delinsGT
ENST00000688158.1:c.*976_*977delinsGT	ENSP00000509254.1:n.*976_*977delinsGT
ENST00000688308.1:c.865_866delinsGT	ENSP00000508752.1:p.Lys289Val
ENST00000688922.1:c.786_787delinsGT
ENST00000693560.1:c.1384_1385delinsGT	ENSP00000509861.1:p.Lys462Val
ENST00000371953.8:c.865_866delinsGT MANE Select	ENSP00000361021.3:p.Lys289Val
ENST00000371953.7:c.865_866delinsGT	ENSP00000361021.3:p.Lys289Val
ENST00000472832.2:c.292_293delinsGT	ENSP00000483066.1:p.Lys98Val
NM_000314.5:c.865_866delinsGT	NP_000305.3:p.Lys289Val
NM_000314.6:c.865_866delinsGT	NP_000305.3:p.Lys289Val
NM_001304717.2:c.1384_1385delinsGT	NP_001291646.2:p.Lys462Val
NM_001304718.1:c.274_275delinsGT	NP_001291647.1:p.Lys92Val
XM_006717926.2:c.820_821delinsGT	XP_006717989.1:p.Lys274Val
XM_011539981.1:c.865_866delinsGT	XP_011538283.1:p.Lys289Val
XM_011539982.1:c.769_770delinsGT	XP_011538284.1:p.Lys257Val
XR_945791.1:n.1435_1436delinsGT
NM_000314.7:c.865_866delinsGT	NP_000305.3:p.Lys289Val
NM_001304717.5:c.1384_1385delinsGT	NP_001291646.4:p.Lys462Val
NM_001304718.2:c.274_275delinsGT	NP_001291647.1:p.Lys92Val
NM_000314.8:c.865_866delinsGT MANE Select	NP_000305.3:p.Lys289Val