Canonical Allele Identifier: CA891838708

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952139_87952141delinsGAT , CM000672.2:g.87952139_87952141delinsGAT	GRCh38
NC_000010.10:g.89711896_89711898delinsGAT , CM000672.1:g.89711896_89711898delinsGAT	GRCh37
NC_000010.9:g.89701876_89701878delinsGAT	NCBI36
NG_007466.2:g.93701_93703delinsGAT , LRG_311:g.93701_93703delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.514_516delinsGAT	ENSP00000514759.2:p.Arg172Asp
ENST00000710265.1:c.514_516delinsGAT	ENSP00000518161.1:p.Arg172Asp
ENST00000472832.3:c.514_516delinsGAT	ENSP00000483066.2:p.Arg172Asp
ENST00000688158.2:n.1249_1251delinsGAT
ENST00000688922.2:c.*344_*346delinsGAT	ENSP00000508742.2:n.*344_*346delinsGAT
ENST00000700021.1:c.469_471delinsGAT	ENSP00000514757.1:p.Arg157Asp
ENST00000700022.1:c.493-5714_493-5712delinsGAT	ENSP00000514758.1:n.493-5714_493-5712delinsGAT
ENST00000700023.1:n.1672_1674delinsGAT
ENST00000700024.1:n.1906_1908delinsGAT
ENST00000700025.1:n.1283_1285delinsGAT
ENST00000700029.1:c.348_350delinsGAT
ENST00000706954.1:c.514_516delinsGAT	ENSP00000516674.1:p.Arg172Asp
ENST00000706955.1:c.*549_*551delinsGAT	ENSP00000516675.1:n.*549_*551delinsGAT
ENST00000686459.1:c.*100_*102delinsGAT	ENSP00000508909.1:n.*100_*102delinsGAT
ENST00000688158.1:c.*625_*627delinsGAT	ENSP00000509254.1:n.*625_*627delinsGAT
ENST00000688308.1:c.514_516delinsGAT	ENSP00000508752.1:p.Arg172Asp
ENST00000688922.1:c.435_437delinsGAT
ENST00000693560.1:c.1033_1035delinsGAT	ENSP00000509861.1:p.Arg345Asp
ENST00000371953.8:c.514_516delinsGAT MANE Select	ENSP00000361021.3:p.Arg172Asp
ENST00000371953.7:c.514_516delinsGAT	ENSP00000361021.3:p.Arg172Asp
NM_000314.5:c.514_516delinsGAT	NP_000305.3:p.Arg172Asp
NM_000314.6:c.514_516delinsGAT	NP_000305.3:p.Arg172Asp
NM_001304717.2:c.1033_1035delinsGAT	NP_001291646.2:p.Arg345Asp
NM_001304718.1:c.-78_-76delinsGAT	NP_001291647.1:n.-78_-76delinsGAT
XM_006717926.2:c.469_471delinsGAT	XP_006717989.1:p.Arg157Asp
XM_011539981.1:c.514_516delinsGAT	XP_011538283.1:p.Arg172Asp
XM_011539982.1:c.418_420delinsGAT	XP_011538284.1:p.Arg140Asp
XR_945789.1:n.1385_1387delinsGAT
XR_945790.1:n.1502_1504delinsGAT
XR_945791.1:n.1205-5714_1205-5712delinsGAT
NM_000314.7:c.514_516delinsGAT	NP_000305.3:p.Arg172Asp
NM_001304717.5:c.1033_1035delinsGAT	NP_001291646.4:p.Arg345Asp
NM_001304718.2:c.-78_-76delinsGAT	NP_001291647.1:n.-78_-76delinsGAT
NM_000314.8:c.514_516delinsGAT MANE Select	NP_000305.3:p.Arg172Asp