Canonical Allele Identifier: CA891834892

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960939_87960941delinsACT , CM000672.2:g.87960939_87960941delinsACT	GRCh38
NC_000010.10:g.89720696_89720698delinsACT , CM000672.1:g.89720696_89720698delinsACT	GRCh37
NC_000010.9:g.89710676_89710678delinsACT	NCBI36
NG_007466.2:g.102501_102503delinsACT , LRG_311:g.102501_102503delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.940_942delinsACT	ENSP00000514759.2:p.Pro314Thr
ENST00000710265.1:c.847_849delinsACT	ENSP00000518161.1:p.Pro283Thr
ENST00000472832.3:c.847_849delinsACT	ENSP00000483066.2:p.Pro283Thr
ENST00000688158.2:n.1582_1584delinsACT
ENST00000688922.2:c.*677_*679delinsACT	ENSP00000508742.2:n.*677_*679delinsACT
ENST00000700021.1:c.802_804delinsACT	ENSP00000514757.1:p.Pro268Thr
ENST00000700022.1:c.*186_*188delinsACT	ENSP00000514758.1:n.*186_*188delinsACT
ENST00000700023.1:n.2005_2007delinsACT
ENST00000700024.1:n.2239_2241delinsACT
ENST00000700025.1:n.1616_1618delinsACT
ENST00000700026.1:n.484_486delinsACT
ENST00000700029.1:c.774_776delinsACT
ENST00000706954.1:c.847_849delinsACT	ENSP00000516674.1:p.Pro283Thr
ENST00000706955.1:c.*882_*884delinsACT	ENSP00000516675.1:n.*882_*884delinsACT
ENST00000686459.1:c.*433_*435delinsACT	ENSP00000508909.1:n.*433_*435delinsACT
ENST00000688158.1:c.*958_*960delinsACT	ENSP00000509254.1:n.*958_*960delinsACT
ENST00000688308.1:c.847_849delinsACT	ENSP00000508752.1:p.Pro283Thr
ENST00000688922.1:c.768_770delinsACT
ENST00000693560.1:c.1366_1368delinsACT	ENSP00000509861.1:p.Pro456Thr
ENST00000371953.8:c.847_849delinsACT MANE Select	ENSP00000361021.3:p.Pro283Thr
ENST00000371953.7:c.847_849delinsACT	ENSP00000361021.3:p.Pro283Thr
ENST00000472832.2:c.274_276delinsACT	ENSP00000483066.1:p.Pro92Thr
NM_000314.5:c.847_849delinsACT	NP_000305.3:p.Pro283Thr
NM_000314.6:c.847_849delinsACT	NP_000305.3:p.Pro283Thr
NM_001304717.2:c.1366_1368delinsACT	NP_001291646.2:p.Pro456Thr
NM_001304718.1:c.256_258delinsACT	NP_001291647.1:p.Pro86Thr
XM_006717926.2:c.802_804delinsACT	XP_006717989.1:p.Pro268Thr
XM_011539981.1:c.847_849delinsACT	XP_011538283.1:p.Pro283Thr
XM_011539982.1:c.751_753delinsACT	XP_011538284.1:p.Pro251Thr
XR_945791.1:n.1417_1419delinsACT
NM_000314.7:c.847_849delinsACT	NP_000305.3:p.Pro283Thr
NM_001304717.5:c.1366_1368delinsACT	NP_001291646.4:p.Pro456Thr
NM_001304718.2:c.256_258delinsACT	NP_001291647.1:p.Pro86Thr
NM_000314.8:c.847_849delinsACT MANE Select	NP_000305.3:p.Pro283Thr