Canonical Allele Identifier: CA891839544

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957903_87957905delinsACT , CM000672.2:g.87957903_87957905delinsACT	GRCh38
NC_000010.10:g.89717660_89717662delinsACT , CM000672.1:g.89717660_89717662delinsACT	GRCh37
NC_000010.9:g.89707640_89707642delinsACT	NCBI36
NG_007466.2:g.99465_99467delinsACT , LRG_311:g.99465_99467delinsACT

Transcript Alleles

HGVS	Amino-acid Change
NM_000314.8:c.685_687delinsACT MANE Select	NP_000305.3:p.Ser229Thr
ENST00000371953.8:c.685_687delinsACT MANE Select	ENSP00000361021.3:p.Ser229Thr
NM_000314.5:c.685_687delinsACT	NP_000305.3:p.Ser229Thr
NM_000314.6:c.685_687delinsACT	NP_000305.3:p.Ser229Thr
NM_000314.7:c.685_687delinsACT	NP_000305.3:p.Ser229Thr
NM_001304717.2:c.1204_1206delinsACT	NP_001291646.2:p.Ser402Thr
NM_001304717.5:c.1204_1206delinsACT	NP_001291646.4:p.Ser402Thr
NM_001304718.1:c.94_96delinsACT	NP_001291647.1:p.Ser32Thr
NM_001304718.2:c.94_96delinsACT	NP_001291647.1:p.Ser32Thr
ENST00000371953.7:c.685_687delinsACT	ENSP00000361021.3:p.Ser229Thr
ENST00000472832.2:c.112_114delinsACT	ENSP00000483066.1:p.Ser38Thr
ENST00000472832.3:c.685_687delinsACT	ENSP00000483066.2:p.Ser229Thr
ENST00000686459.1:c.*271_*273delinsACT	ENSP00000508909.1:n.*271_*273delinsACT
ENST00000688158.1:c.*796_*798delinsACT	ENSP00000509254.1:n.*796_*798delinsACT
ENST00000688158.2:n.1420_1422delinsACT
ENST00000688308.1:c.685_687delinsACT	ENSP00000508752.1:p.Ser229Thr
ENST00000688922.1:c.606_608delinsACT
ENST00000688922.2:c.*515_*517delinsACT	ENSP00000508742.2:n.*515_*517delinsACT
ENST00000693560.1:c.1204_1206delinsACT	ENSP00000509861.1:p.Ser402Thr
ENST00000700021.1:c.640_642delinsACT	ENSP00000514757.1:p.Ser214Thr
ENST00000700022.1:c.*24_*26delinsACT	ENSP00000514758.1:n.*24_*26delinsACT
ENST00000700023.1:n.1843_1845delinsACT
ENST00000700024.1:n.2077_2079delinsACT
ENST00000700025.1:n.1454_1456delinsACT
ENST00000700026.1:n.322_324delinsACT
ENST00000700029.1:c.519_521delinsACT
ENST00000700029.2:c.685_687delinsACT	ENSP00000514759.2:p.Ser229Thr
ENST00000706954.1:c.685_687delinsACT	ENSP00000516674.1:p.Ser229Thr
ENST00000706955.1:c.*720_*722delinsACT	ENSP00000516675.1:n.*720_*722delinsACT
ENST00000710265.1:c.685_687delinsACT	ENSP00000518161.1:p.Ser229Thr
XM_006717926.2:c.640_642delinsACT	XP_006717989.1:p.Ser214Thr
XM_011539981.1:c.685_687delinsACT	XP_011538283.1:p.Ser229Thr
XM_011539982.1:c.589_591delinsACT	XP_011538284.1:p.Ser197Thr
XR_945791.1:n.1255_1257delinsACT