Canonical Allele Identifier: CA891835797

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960996_87960998delinsGAA , CM000672.2:g.87960996_87960998delinsGAA	GRCh38
NC_000010.10:g.89720753_89720755delinsGAA , CM000672.1:g.89720753_89720755delinsGAA	GRCh37
NC_000010.9:g.89710733_89710735delinsGAA	NCBI36
NG_007466.2:g.102558_102560delinsGAA , LRG_311:g.102558_102560delinsGAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.997_999delinsGAA	ENSP00000514759.2:p.Ser333Glu
ENST00000710265.1:c.904_906delinsGAA	ENSP00000518161.1:p.Ser302Glu
ENST00000472832.3:c.904_906delinsGAA	ENSP00000483066.2:p.Ser302Glu
ENST00000688158.2:n.1639_1641delinsGAA
ENST00000688922.2:c.*734_*736delinsGAA	ENSP00000508742.2:n.*734_*736delinsGAA
ENST00000700021.1:c.859_861delinsGAA	ENSP00000514757.1:p.Ser287Glu
ENST00000700022.1:c.*243_*245delinsGAA	ENSP00000514758.1:n.*243_*245delinsGAA
ENST00000700023.1:n.2062_2064delinsGAA
ENST00000700024.1:n.2296_2298delinsGAA
ENST00000700025.1:n.1673_1675delinsGAA
ENST00000700026.1:n.541_543delinsGAA
ENST00000706954.1:c.904_906delinsGAA	ENSP00000516674.1:p.Ser302Glu
ENST00000706955.1:c.*939_*941delinsGAA	ENSP00000516675.1:n.*939_*941delinsGAA
ENST00000686459.1:c.*490_*492delinsGAA	ENSP00000508909.1:n.*490_*492delinsGAA
ENST00000688158.1:c.*1015_*1017delinsGAA	ENSP00000509254.1:n.*1015_*1017delinsGAA
ENST00000688308.1:c.904_906delinsGAA	ENSP00000508752.1:p.Ser302Glu
ENST00000688922.1:c.825_827delinsGAA
ENST00000693560.1:c.1423_1425delinsGAA	ENSP00000509861.1:p.Ser475Glu
ENST00000371953.8:c.904_906delinsGAA MANE Select	ENSP00000361021.3:p.Ser302Glu
ENST00000371953.7:c.904_906delinsGAA	ENSP00000361021.3:p.Ser302Glu
ENST00000472832.2:c.331_333delinsGAA	ENSP00000483066.1:p.Ser111Glu
NM_000314.5:c.904_906delinsGAA	NP_000305.3:p.Ser302Glu
NM_000314.6:c.904_906delinsGAA	NP_000305.3:p.Ser302Glu
NM_001304717.2:c.1423_1425delinsGAA	NP_001291646.2:p.Ser475Glu
NM_001304718.1:c.313_315delinsGAA	NP_001291647.1:p.Ser105Glu
XM_006717926.2:c.859_861delinsGAA	XP_006717989.1:p.Ser287Glu
XM_011539981.1:c.904_906delinsGAA	XP_011538283.1:p.Ser302Glu
XM_011539982.1:c.808_810delinsGAA	XP_011538284.1:p.Ser270Glu
XR_945791.1:n.1474_1476delinsGAA
NM_000314.7:c.904_906delinsGAA	NP_000305.3:p.Ser302Glu
NM_001304717.5:c.1423_1425delinsGAA	NP_001291646.4:p.Ser475Glu
NM_001304718.2:c.313_315delinsGAA	NP_001291647.1:p.Ser105Glu
NM_000314.8:c.904_906delinsGAA MANE Select	NP_000305.3:p.Ser302Glu