Canonical Allele Identifier: CA891837955

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933168_87933169delinsTA , CM000672.2:g.87933168_87933169delinsTA	GRCh38
NC_000010.10:g.89692925_89692926delinsTA , CM000672.1:g.89692925_89692926delinsTA	GRCh37
NC_000010.9:g.89682905_89682906delinsTA	NCBI36
NG_007466.2:g.74730_74731delinsTA , LRG_311:g.74730_74731delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.409_410delinsTA	ENSP00000514759.2:p.Ala137Ter
ENST00000710265.1:c.409_410delinsTA	ENSP00000518161.1:p.Ala137Ter
ENST00000472832.3:c.409_410delinsTA	ENSP00000483066.2:p.Ala137Ter
ENST00000688158.2:n.1144_1145delinsTA
ENST00000688922.2:c.*239_*240delinsTA	ENSP00000508742.2:n.*239_*240delinsTA
ENST00000700021.1:c.364_365delinsTA	ENSP00000514757.1:p.Ala122Ter
ENST00000700022.1:c.409_410delinsTA	ENSP00000514758.1:p.Ala137Ter
ENST00000700029.1:c.243_244delinsTA
ENST00000706954.1:c.409_410delinsTA	ENSP00000516674.1:p.Ala137Ter
ENST00000706955.1:c.*444_*445delinsTA	ENSP00000516675.1:n.*444_*445delinsTA
ENST00000686459.1:c.409_410delinsTA	ENSP00000508909.1:p.Ala137Ter
ENST00000688158.1:c.*520_*521delinsTA	ENSP00000509254.1:n.*520_*521delinsTA
ENST00000688308.1:c.409_410delinsTA	ENSP00000508752.1:p.Ala137Ter
ENST00000688922.1:c.330_331delinsTA
ENST00000693560.1:c.928_929delinsTA	ENSP00000509861.1:p.Ala310Ter
ENST00000371953.8:c.409_410delinsTA MANE Select	ENSP00000361021.3:p.Ala137Ter
ENST00000371953.7:c.409_410delinsTA	ENSP00000361021.3:p.Ala137Ter
ENST00000498703.1:n.235_236delinsTA
ENST00000610634.1:c.307_308delinsTA	ENSP00000477517.1:p.Ala103Ter
NM_000314.5:c.409_410delinsTA	NP_000305.3:p.Ala137Ter
NM_000314.6:c.409_410delinsTA	NP_000305.3:p.Ala137Ter
NM_001304717.2:c.928_929delinsTA	NP_001291646.2:p.Ala310Ter
NM_001304718.1:c.-342_-341delinsTA	NP_001291647.1:n.-342_-341delinsTA
XM_006717926.2:c.364_365delinsTA	XP_006717989.1:p.Ala122Ter
XM_011539981.1:c.409_410delinsTA	XP_011538283.1:p.Ala137Ter
XM_011539982.1:c.313_314delinsTA	XP_011538284.1:p.Ala105Ter
XR_945789.1:n.1121_1122delinsTA
XR_945790.1:n.1121_1122delinsTA
XR_945791.1:n.1121_1122delinsTA
NM_000314.7:c.409_410delinsTA	NP_000305.3:p.Ala137Ter
NM_001304717.5:c.928_929delinsTA	NP_001291646.4:p.Ala310Ter
NM_001304718.2:c.-342_-341delinsTA	NP_001291647.1:n.-342_-341delinsTA
NM_000314.8:c.409_410delinsTA MANE Select	NP_000305.3:p.Ala137Ter