Canonical Allele Identifier: CA891838057

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965428_87965430delinsTTG , CM000672.2:g.87965428_87965430delinsTTG	GRCh38
NC_000010.10:g.89725185_89725187delinsTTG , CM000672.1:g.89725185_89725187delinsTTG	GRCh37
NC_000010.9:g.89715165_89715167delinsTTG	NCBI36
NG_007466.2:g.106990_106992delinsTTG , LRG_311:g.106990_106992delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1261_1263delinsTTG	ENSP00000514759.2:p.Glu421Leu
ENST00000710265.1:c.*197_*199delinsTTG	ENSP00000518161.1:n.*197_*199delinsTTG
ENST00000688158.2:n.1903_1905delinsTTG
ENST00000688922.2:c.*998_*1000delinsTTG	ENSP00000508742.2:n.*998_*1000delinsTTG
ENST00000700021.1:c.1123_1125delinsTTG	ENSP00000514757.1:p.Glu375Leu
ENST00000700022.1:c.*507_*509delinsTTG	ENSP00000514758.1:n.*507_*509delinsTTG
ENST00000700023.1:n.2326_2328delinsTTG
ENST00000700024.1:n.2560_2562delinsTTG
ENST00000706954.1:c.1168_1170delinsTTG	ENSP00000516674.1:p.Glu390Leu
ENST00000706955.1:c.*1203_*1205delinsTTG	ENSP00000516675.1:n.*1203_*1205delinsTTG
ENST00000686459.1:c.*754_*756delinsTTG	ENSP00000508909.1:n.*754_*756delinsTTG
ENST00000688158.1:c.*1279_*1281delinsTTG	ENSP00000509254.1:n.*1279_*1281delinsTTG
ENST00000688308.1:c.1168_1170delinsTTG	ENSP00000508752.1:p.Glu390Leu
ENST00000688922.1:c.1089_1091delinsTTG
ENST00000693560.1:c.1687_1689delinsTTG	ENSP00000509861.1:p.Glu563Leu
ENST00000371953.8:c.1168_1170delinsTTG MANE Select	ENSP00000361021.3:p.Glu390Leu
ENST00000371953.7:c.1168_1170delinsTTG	ENSP00000361021.3:p.Glu390Leu
NM_000314.5:c.1168_1170delinsTTG	NP_000305.3:p.Glu390Leu
NM_000314.6:c.1168_1170delinsTTG	NP_000305.3:p.Glu390Leu
NM_001304717.2:c.1687_1689delinsTTG	NP_001291646.2:p.Glu563Leu
NM_001304718.1:c.577_579delinsTTG	NP_001291647.1:p.Glu193Leu
XM_006717926.2:c.1123_1125delinsTTG	XP_006717989.1:p.Glu375Leu
XM_011539982.1:c.1072_1074delinsTTG	XP_011538284.1:p.Glu358Leu
XR_945791.1:n.1738_1740delinsTTG
NM_000314.7:c.1168_1170delinsTTG	NP_000305.3:p.Glu390Leu
NM_001304717.5:c.1687_1689delinsTTG	NP_001291646.4:p.Glu563Leu
NM_001304718.2:c.577_579delinsTTG	NP_001291647.1:p.Glu193Leu
NM_000314.8:c.1168_1170delinsTTG MANE Select	NP_000305.3:p.Glu390Leu