Canonical Allele Identifier: CA891837017

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965305_87965307delinsTTT , CM000672.2:g.87965305_87965307delinsTTT	GRCh38
NC_000010.10:g.89725062_89725064delinsTTT , CM000672.1:g.89725062_89725064delinsTTT	GRCh37
NC_000010.9:g.89715042_89715044delinsTTT	NCBI36
NG_007466.2:g.106867_106869delinsTTT , LRG_311:g.106867_106869delinsTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1138_1140delinsTTT	ENSP00000514759.2:p.Lys380Phe
ENST00000710265.1:c.*74_*76delinsTTT	ENSP00000518161.1:n.*74_*76delinsTTT
ENST00000688158.2:n.1780_1782delinsTTT
ENST00000688922.2:c.*875_*877delinsTTT	ENSP00000508742.2:n.*875_*877delinsTTT
ENST00000700021.1:c.1000_1002delinsTTT	ENSP00000514757.1:p.Lys334Phe
ENST00000700022.1:c.*384_*386delinsTTT	ENSP00000514758.1:n.*384_*386delinsTTT
ENST00000700023.1:n.2203_2205delinsTTT
ENST00000700024.1:n.2437_2439delinsTTT
ENST00000706954.1:c.1045_1047delinsTTT	ENSP00000516674.1:p.Lys349Phe
ENST00000706955.1:c.*1080_*1082delinsTTT	ENSP00000516675.1:n.*1080_*1082delinsTTT
ENST00000686459.1:c.*631_*633delinsTTT	ENSP00000508909.1:n.*631_*633delinsTTT
ENST00000688158.1:c.*1156_*1158delinsTTT	ENSP00000509254.1:n.*1156_*1158delinsTTT
ENST00000688308.1:c.1045_1047delinsTTT	ENSP00000508752.1:p.Lys349Phe
ENST00000688922.1:c.966_968delinsTTT
ENST00000693560.1:c.1564_1566delinsTTT	ENSP00000509861.1:p.Lys522Phe
ENST00000371953.8:c.1045_1047delinsTTT MANE Select	ENSP00000361021.3:p.Lys349Phe
ENST00000371953.7:c.1045_1047delinsTTT	ENSP00000361021.3:p.Lys349Phe
NM_000314.5:c.1045_1047delinsTTT	NP_000305.3:p.Lys349Phe
NM_000314.6:c.1045_1047delinsTTT	NP_000305.3:p.Lys349Phe
NM_001304717.2:c.1564_1566delinsTTT	NP_001291646.2:p.Lys522Phe
NM_001304718.1:c.454_456delinsTTT	NP_001291647.1:p.Lys152Phe
XM_006717926.2:c.1000_1002delinsTTT	XP_006717989.1:p.Lys334Phe
XM_011539982.1:c.949_951delinsTTT	XP_011538284.1:p.Lys317Phe
XR_945791.1:n.1615_1617delinsTTT
NM_000314.7:c.1045_1047delinsTTT	NP_000305.3:p.Lys349Phe
NM_001304717.5:c.1564_1566delinsTTT	NP_001291646.4:p.Lys522Phe
NM_001304718.2:c.454_456delinsTTT	NP_001291647.1:p.Lys152Phe
NM_000314.8:c.1045_1047delinsTTT MANE Select	NP_000305.3:p.Lys349Phe