Canonical Allele Identifier: CA891837697

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933147_87933149delinsTTG , CM000672.2:g.87933147_87933149delinsTTG	GRCh38
NC_000010.10:g.89692904_89692906delinsTTG , CM000672.1:g.89692904_89692906delinsTTG	GRCh37
NC_000010.9:g.89682884_89682886delinsTTG	NCBI36
NG_007466.2:g.74709_74711delinsTTG , LRG_311:g.74709_74711delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.388_390delinsTTG	ENSP00000514759.2:p.Arg130Leu
ENST00000710265.1:c.388_390delinsTTG	ENSP00000518161.1:p.Arg130Leu
ENST00000472832.3:c.388_390delinsTTG	ENSP00000483066.2:p.Arg130Leu
ENST00000688158.2:n.1123_1125delinsTTG
ENST00000688922.2:c.*218_*220delinsTTG	ENSP00000508742.2:n.*218_*220delinsTTG
ENST00000700021.1:c.343_345delinsTTG	ENSP00000514757.1:p.Arg115Leu
ENST00000700022.1:c.388_390delinsTTG	ENSP00000514758.1:p.Arg130Leu
ENST00000700029.1:c.222_224delinsTTG
ENST00000706954.1:c.388_390delinsTTG	ENSP00000516674.1:p.Arg130Leu
ENST00000706955.1:c.*423_*425delinsTTG	ENSP00000516675.1:n.*423_*425delinsTTG
ENST00000686459.1:c.388_390delinsTTG	ENSP00000508909.1:p.Arg130Leu
ENST00000688158.1:c.*499_*501delinsTTG	ENSP00000509254.1:n.*499_*501delinsTTG
ENST00000688308.1:c.388_390delinsTTG	ENSP00000508752.1:p.Arg130Leu
ENST00000688922.1:c.309_311delinsTTG
ENST00000693560.1:c.907_909delinsTTG	ENSP00000509861.1:p.Arg303Leu
ENST00000371953.8:c.388_390delinsTTG MANE Select	ENSP00000361021.3:p.Arg130Leu
ENST00000371953.7:c.388_390delinsTTG	ENSP00000361021.3:p.Arg130Leu
ENST00000498703.1:n.214_216delinsTTG
ENST00000610634.1:c.286_288delinsTTG	ENSP00000477517.1:p.Arg96Leu
NM_000314.5:c.388_390delinsTTG	NP_000305.3:p.Arg130Leu
NM_000314.6:c.388_390delinsTTG	NP_000305.3:p.Arg130Leu
NM_001304717.2:c.907_909delinsTTG	NP_001291646.2:p.Arg303Leu
NM_001304718.1:c.-363_-361delinsTTG	NP_001291647.1:n.-363_-361delinsTTG
XM_006717926.2:c.343_345delinsTTG	XP_006717989.1:p.Arg115Leu
XM_011539981.1:c.388_390delinsTTG	XP_011538283.1:p.Arg130Leu
XM_011539982.1:c.292_294delinsTTG	XP_011538284.1:p.Arg98Leu
XR_945789.1:n.1100_1102delinsTTG
XR_945790.1:n.1100_1102delinsTTG
XR_945791.1:n.1100_1102delinsTTG
NM_000314.7:c.388_390delinsTTG	NP_000305.3:p.Arg130Leu
NM_001304717.5:c.907_909delinsTTG	NP_001291646.4:p.Arg303Leu
NM_001304718.2:c.-363_-361delinsTTG	NP_001291647.1:n.-363_-361delinsTTG
NM_000314.8:c.388_390delinsTTG MANE Select	NP_000305.3:p.Arg130Leu