Canonical Allele Identifier: CA891835165

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960957_87960958delinsCC , CM000672.2:g.87960957_87960958delinsCC	GRCh38
NC_000010.10:g.89720714_89720715delinsCC , CM000672.1:g.89720714_89720715delinsCC	GRCh37
NC_000010.9:g.89710694_89710695delinsCC	NCBI36
NG_007466.2:g.102519_102520delinsCC , LRG_311:g.102519_102520delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.958_959delinsCC	ENSP00000514759.2:p.Lys320Pro
ENST00000710265.1:c.865_866delinsCC	ENSP00000518161.1:p.Lys289Pro
ENST00000472832.3:c.865_866delinsCC	ENSP00000483066.2:p.Lys289Pro
ENST00000688158.2:n.1600_1601delinsCC
ENST00000688922.2:c.*695_*696delinsCC	ENSP00000508742.2:n.*695_*696delinsCC
ENST00000700021.1:c.820_821delinsCC	ENSP00000514757.1:p.Lys274Pro
ENST00000700022.1:c.*204_*205delinsCC	ENSP00000514758.1:n.*204_*205delinsCC
ENST00000700023.1:n.2023_2024delinsCC
ENST00000700024.1:n.2257_2258delinsCC
ENST00000700025.1:n.1634_1635delinsCC
ENST00000700026.1:n.502_503delinsCC
ENST00000700029.1:c.792_793delinsCC
ENST00000706954.1:c.865_866delinsCC	ENSP00000516674.1:p.Lys289Pro
ENST00000706955.1:c.*900_*901delinsCC	ENSP00000516675.1:n.*900_*901delinsCC
ENST00000686459.1:c.*451_*452delinsCC	ENSP00000508909.1:n.*451_*452delinsCC
ENST00000688158.1:c.*976_*977delinsCC	ENSP00000509254.1:n.*976_*977delinsCC
ENST00000688308.1:c.865_866delinsCC	ENSP00000508752.1:p.Lys289Pro
ENST00000688922.1:c.786_787delinsCC
ENST00000693560.1:c.1384_1385delinsCC	ENSP00000509861.1:p.Lys462Pro
ENST00000371953.8:c.865_866delinsCC MANE Select	ENSP00000361021.3:p.Lys289Pro
ENST00000371953.7:c.865_866delinsCC	ENSP00000361021.3:p.Lys289Pro
ENST00000472832.2:c.292_293delinsCC	ENSP00000483066.1:p.Lys98Pro
NM_000314.5:c.865_866delinsCC	NP_000305.3:p.Lys289Pro
NM_000314.6:c.865_866delinsCC	NP_000305.3:p.Lys289Pro
NM_001304717.2:c.1384_1385delinsCC	NP_001291646.2:p.Lys462Pro
NM_001304718.1:c.274_275delinsCC	NP_001291647.1:p.Lys92Pro
XM_006717926.2:c.820_821delinsCC	XP_006717989.1:p.Lys274Pro
XM_011539981.1:c.865_866delinsCC	XP_011538283.1:p.Lys289Pro
XM_011539982.1:c.769_770delinsCC	XP_011538284.1:p.Lys257Pro
XR_945791.1:n.1435_1436delinsCC
NM_000314.7:c.865_866delinsCC	NP_000305.3:p.Lys289Pro
NM_001304717.5:c.1384_1385delinsCC	NP_001291646.4:p.Lys462Pro
NM_001304718.2:c.274_275delinsCC	NP_001291647.1:p.Lys92Pro
NM_000314.8:c.865_866delinsCC MANE Select	NP_000305.3:p.Lys289Pro