Canonical Allele Identifier: CA891840154

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960894_87960896delinsACT , CM000672.2:g.87960894_87960896delinsACT	GRCh38
NC_000010.10:g.89720651_89720653delinsACT , CM000672.1:g.89720651_89720653delinsACT	GRCh37
NC_000010.9:g.89710631_89710633delinsACT	NCBI36
NG_007466.2:g.102456_102458delinsACT , LRG_311:g.102456_102458delinsACT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.895_897delinsACT	ENSP00000514759.2:p.Asp299Thr
ENST00000710265.1:c.802_804delinsACT	ENSP00000518161.1:p.Asp268Thr
ENST00000472832.3:c.802_804delinsACT	ENSP00000483066.2:p.Asp268Thr
ENST00000688158.2:n.1537_1539delinsACT
ENST00000688922.2:c.*632_*634delinsACT	ENSP00000508742.2:n.*632_*634delinsACT
ENST00000700021.1:c.757_759delinsACT	ENSP00000514757.1:p.Asp253Thr
ENST00000700022.1:c.*141_*143delinsACT	ENSP00000514758.1:n.*141_*143delinsACT
ENST00000700023.1:n.1960_1962delinsACT
ENST00000700024.1:n.2194_2196delinsACT
ENST00000700025.1:n.1571_1573delinsACT
ENST00000700026.1:n.439_441delinsACT
ENST00000700029.1:c.729_731delinsACT
ENST00000706954.1:c.802_804delinsACT	ENSP00000516674.1:p.Asp268Thr
ENST00000706955.1:c.*837_*839delinsACT	ENSP00000516675.1:n.*837_*839delinsACT
ENST00000686459.1:c.*388_*390delinsACT	ENSP00000508909.1:n.*388_*390delinsACT
ENST00000688158.1:c.*913_*915delinsACT	ENSP00000509254.1:n.*913_*915delinsACT
ENST00000688308.1:c.802_804delinsACT	ENSP00000508752.1:p.Asp268Thr
ENST00000688922.1:c.723_725delinsACT
ENST00000693560.1:c.1321_1323delinsACT	ENSP00000509861.1:p.Asp441Thr
ENST00000371953.8:c.802_804delinsACT MANE Select	ENSP00000361021.3:p.Asp268Thr
ENST00000371953.7:c.802_804delinsACT	ENSP00000361021.3:p.Asp268Thr
ENST00000472832.2:c.229_231delinsACT	ENSP00000483066.1:p.Asp77Thr
NM_000314.5:c.802_804delinsACT	NP_000305.3:p.Asp268Thr
NM_000314.6:c.802_804delinsACT	NP_000305.3:p.Asp268Thr
NM_001304717.2:c.1321_1323delinsACT	NP_001291646.2:p.Asp441Thr
NM_001304718.1:c.211_213delinsACT	NP_001291647.1:p.Asp71Thr
XM_006717926.2:c.757_759delinsACT	XP_006717989.1:p.Asp253Thr
XM_011539981.1:c.802_804delinsACT	XP_011538283.1:p.Asp268Thr
XM_011539982.1:c.706_708delinsACT	XP_011538284.1:p.Asp236Thr
XR_945791.1:n.1372_1374delinsACT
NM_000314.7:c.802_804delinsACT	NP_000305.3:p.Asp268Thr
NM_001304717.5:c.1321_1323delinsACT	NP_001291646.4:p.Asp441Thr
NM_001304718.2:c.211_213delinsACT	NP_001291647.1:p.Asp71Thr
NM_000314.8:c.802_804delinsACT MANE Select	NP_000305.3:p.Asp268Thr