Canonical Allele Identifier: CA891837294

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965335_87965336delinsTA , CM000672.2:g.87965335_87965336delinsTA	GRCh38
NC_000010.10:g.89725092_89725093delinsTA , CM000672.1:g.89725092_89725093delinsTA	GRCh37
NC_000010.9:g.89715072_89715073delinsTA	NCBI36
NG_007466.2:g.106897_106898delinsTA , LRG_311:g.106897_106898delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1168_1169delinsTA	ENSP00000514759.2:p.Ala390Tyr
ENST00000710265.1:c.*104_*105delinsTA	ENSP00000518161.1:n.*104_*105delinsTA
ENST00000688158.2:n.1810_1811delinsTA
ENST00000688922.2:c.*905_*906delinsTA	ENSP00000508742.2:n.*905_*906delinsTA
ENST00000700021.1:c.1030_1031delinsTA	ENSP00000514757.1:p.Ala344Tyr
ENST00000700022.1:c.*414_*415delinsTA	ENSP00000514758.1:n.*414_*415delinsTA
ENST00000700023.1:n.2233_2234delinsTA
ENST00000700024.1:n.2467_2468delinsTA
ENST00000706954.1:c.1075_1076delinsTA	ENSP00000516674.1:p.Ala359Tyr
ENST00000706955.1:c.*1110_*1111delinsTA	ENSP00000516675.1:n.*1110_*1111delinsTA
ENST00000686459.1:c.*661_*662delinsTA	ENSP00000508909.1:n.*661_*662delinsTA
ENST00000688158.1:c.*1186_*1187delinsTA	ENSP00000509254.1:n.*1186_*1187delinsTA
ENST00000688308.1:c.1075_1076delinsTA	ENSP00000508752.1:p.Ala359Tyr
ENST00000688922.1:c.996_997delinsTA
ENST00000693560.1:c.1594_1595delinsTA	ENSP00000509861.1:p.Ala532Tyr
ENST00000371953.8:c.1075_1076delinsTA MANE Select	ENSP00000361021.3:p.Ala359Tyr
ENST00000371953.7:c.1075_1076delinsTA	ENSP00000361021.3:p.Ala359Tyr
NM_000314.5:c.1075_1076delinsTA	NP_000305.3:p.Ala359Tyr
NM_000314.6:c.1075_1076delinsTA	NP_000305.3:p.Ala359Tyr
NM_001304717.2:c.1594_1595delinsTA	NP_001291646.2:p.Ala532Tyr
NM_001304718.1:c.484_485delinsTA	NP_001291647.1:p.Ala162Tyr
XM_006717926.2:c.1030_1031delinsTA	XP_006717989.1:p.Ala344Tyr
XM_011539982.1:c.979_980delinsTA	XP_011538284.1:p.Ala327Tyr
XR_945791.1:n.1645_1646delinsTA
NM_000314.7:c.1075_1076delinsTA	NP_000305.3:p.Ala359Tyr
NM_001304717.5:c.1594_1595delinsTA	NP_001291646.4:p.Ala532Tyr
NM_001304718.2:c.484_485delinsTA	NP_001291647.1:p.Ala162Tyr
NM_000314.8:c.1075_1076delinsTA MANE Select	NP_000305.3:p.Ala359Tyr