Canonical Allele Identifier: CA891839400

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957873_87957875delinsTTT , CM000672.2:g.87957873_87957875delinsTTT	GRCh38
NC_000010.10:g.89717630_89717632delinsTTT , CM000672.1:g.89717630_89717632delinsTTT	GRCh37
NC_000010.9:g.89707610_89707612delinsTTT	NCBI36
NG_007466.2:g.99435_99437delinsTTT , LRG_311:g.99435_99437delinsTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.655_657delinsTTT	ENSP00000514759.2:p.Gln219Phe
ENST00000710265.1:c.655_657delinsTTT	ENSP00000518161.1:p.Gln219Phe
ENST00000472832.3:c.655_657delinsTTT	ENSP00000483066.2:p.Gln219Phe
ENST00000688158.2:n.1390_1392delinsTTT
ENST00000688922.2:c.*485_*487delinsTTT	ENSP00000508742.2:n.*485_*487delinsTTT
ENST00000700021.1:c.610_612delinsTTT	ENSP00000514757.1:p.Gln204Phe
ENST00000700022.1:c.513_515delinsTTT	ENSP00000514758.1:p.Ser172Phe
ENST00000700023.1:n.1813_1815delinsTTT
ENST00000700024.1:n.2047_2049delinsTTT
ENST00000700025.1:n.1424_1426delinsTTT
ENST00000700026.1:n.292_294delinsTTT
ENST00000700029.1:c.489_491delinsTTT
ENST00000706954.1:c.655_657delinsTTT	ENSP00000516674.1:p.Gln219Phe
ENST00000706955.1:c.*690_*692delinsTTT	ENSP00000516675.1:n.*690_*692delinsTTT
ENST00000686459.1:c.*241_*243delinsTTT	ENSP00000508909.1:n.*241_*243delinsTTT
ENST00000688158.1:c.*766_*768delinsTTT	ENSP00000509254.1:n.*766_*768delinsTTT
ENST00000688308.1:c.655_657delinsTTT	ENSP00000508752.1:p.Gln219Phe
ENST00000688922.1:c.576_578delinsTTT
ENST00000693560.1:c.1174_1176delinsTTT	ENSP00000509861.1:p.Gln392Phe
ENST00000371953.8:c.655_657delinsTTT MANE Select	ENSP00000361021.3:p.Gln219Phe
ENST00000371953.7:c.655_657delinsTTT	ENSP00000361021.3:p.Gln219Phe
ENST00000472832.2:c.82_84delinsTTT	ENSP00000483066.1:p.Gln28Phe
NM_000314.5:c.655_657delinsTTT	NP_000305.3:p.Gln219Phe
NM_000314.6:c.655_657delinsTTT	NP_000305.3:p.Gln219Phe
NM_001304717.2:c.1174_1176delinsTTT	NP_001291646.2:p.Gln392Phe
NM_001304718.1:c.64_66delinsTTT	NP_001291647.1:p.Gln22Phe
XM_006717926.2:c.610_612delinsTTT	XP_006717989.1:p.Gln204Phe
XM_011539981.1:c.655_657delinsTTT	XP_011538283.1:p.Gln219Phe
XM_011539982.1:c.559_561delinsTTT	XP_011538284.1:p.Gln187Phe
XR_945791.1:n.1225_1227delinsTTT
NM_000314.7:c.655_657delinsTTT	NP_000305.3:p.Gln219Phe
NM_001304717.5:c.1174_1176delinsTTT	NP_001291646.4:p.Gln392Phe
NM_001304718.2:c.64_66delinsTTT	NP_001291647.1:p.Gln22Phe
NM_000314.8:c.655_657delinsTTT MANE Select	NP_000305.3:p.Gln219Phe