Canonical Allele Identifier: CA891839394

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957873_87957875delinsACT , CM000672.2:g.87957873_87957875delinsACT	GRCh38
NC_000010.10:g.89717630_89717632delinsACT , CM000672.1:g.89717630_89717632delinsACT	GRCh37
NC_000010.9:g.89707610_89707612delinsACT	NCBI36
NG_007466.2:g.99435_99437delinsACT , LRG_311:g.99435_99437delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.655_657delinsACT	ENSP00000514759.2:p.Gln219Thr
ENST00000710265.1:c.655_657delinsACT	ENSP00000518161.1:p.Gln219Thr
ENST00000472832.3:c.655_657delinsACT	ENSP00000483066.2:p.Gln219Thr
ENST00000688158.2:n.1390_1392delinsACT
ENST00000688922.2:c.*485_*487delinsACT	ENSP00000508742.2:n.*485_*487delinsACT
ENST00000700021.1:c.610_612delinsACT	ENSP00000514757.1:p.Gln204Thr
ENST00000700022.1:c.513_515delinsACT	ENSP00000514758.1:p.Ser172Leu
ENST00000700023.1:n.1813_1815delinsACT
ENST00000700024.1:n.2047_2049delinsACT
ENST00000700025.1:n.1424_1426delinsACT
ENST00000700026.1:n.292_294delinsACT
ENST00000700029.1:c.489_491delinsACT
ENST00000706954.1:c.655_657delinsACT	ENSP00000516674.1:p.Gln219Thr
ENST00000706955.1:c.*690_*692delinsACT	ENSP00000516675.1:n.*690_*692delinsACT
ENST00000686459.1:c.*241_*243delinsACT	ENSP00000508909.1:n.*241_*243delinsACT
ENST00000688158.1:c.*766_*768delinsACT	ENSP00000509254.1:n.*766_*768delinsACT
ENST00000688308.1:c.655_657delinsACT	ENSP00000508752.1:p.Gln219Thr
ENST00000688922.1:c.576_578delinsACT
ENST00000693560.1:c.1174_1176delinsACT	ENSP00000509861.1:p.Gln392Thr
ENST00000371953.8:c.655_657delinsACT MANE Select	ENSP00000361021.3:p.Gln219Thr
ENST00000371953.7:c.655_657delinsACT	ENSP00000361021.3:p.Gln219Thr
ENST00000472832.2:c.82_84delinsACT	ENSP00000483066.1:p.Gln28Thr
NM_000314.5:c.655_657delinsACT	NP_000305.3:p.Gln219Thr
NM_000314.6:c.655_657delinsACT	NP_000305.3:p.Gln219Thr
NM_001304717.2:c.1174_1176delinsACT	NP_001291646.2:p.Gln392Thr
NM_001304718.1:c.64_66delinsACT	NP_001291647.1:p.Gln22Thr
XM_006717926.2:c.610_612delinsACT	XP_006717989.1:p.Gln204Thr
XM_011539981.1:c.655_657delinsACT	XP_011538283.1:p.Gln219Thr
XM_011539982.1:c.559_561delinsACT	XP_011538284.1:p.Gln187Thr
XR_945791.1:n.1225_1227delinsACT
NM_000314.7:c.655_657delinsACT	NP_000305.3:p.Gln219Thr
NM_001304717.5:c.1174_1176delinsACT	NP_001291646.4:p.Gln392Thr
NM_001304718.2:c.64_66delinsACT	NP_001291647.1:p.Gln22Thr
NM_000314.8:c.655_657delinsACT MANE Select	NP_000305.3:p.Gln219Thr