Canonical Allele Identifier: CA891841176

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960987_87960988delinsCG , CM000672.2:g.87960987_87960988delinsCG	GRCh38
NC_000010.10:g.89720744_89720745delinsCG , CM000672.1:g.89720744_89720745delinsCG	GRCh37
NC_000010.9:g.89710724_89710725delinsCG	NCBI36
NG_007466.2:g.102549_102550delinsCG , LRG_311:g.102549_102550delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.988_989delinsCG	ENSP00000514759.2:p.Glu330Arg
ENST00000710265.1:c.895_896delinsCG	ENSP00000518161.1:p.Glu299Arg
ENST00000472832.3:c.895_896delinsCG	ENSP00000483066.2:p.Glu299Arg
ENST00000688158.2:n.1630_1631delinsCG
ENST00000688922.2:c.*725_*726delinsCG	ENSP00000508742.2:n.*725_*726delinsCG
ENST00000700021.1:c.850_851delinsCG	ENSP00000514757.1:p.Glu284Arg
ENST00000700022.1:c.*234_*235delinsCG	ENSP00000514758.1:n.*234_*235delinsCG
ENST00000700023.1:n.2053_2054delinsCG
ENST00000700024.1:n.2287_2288delinsCG
ENST00000700025.1:n.1664_1665delinsCG
ENST00000700026.1:n.532_533delinsCG
ENST00000706954.1:c.895_896delinsCG	ENSP00000516674.1:p.Glu299Arg
ENST00000706955.1:c.*930_*931delinsCG	ENSP00000516675.1:n.*930_*931delinsCG
ENST00000686459.1:c.*481_*482delinsCG	ENSP00000508909.1:n.*481_*482delinsCG
ENST00000688158.1:c.*1006_*1007delinsCG	ENSP00000509254.1:n.*1006_*1007delinsCG
ENST00000688308.1:c.895_896delinsCG	ENSP00000508752.1:p.Glu299Arg
ENST00000688922.1:c.816_817delinsCG
ENST00000693560.1:c.1414_1415delinsCG	ENSP00000509861.1:p.Glu472Arg
ENST00000371953.8:c.895_896delinsCG MANE Select	ENSP00000361021.3:p.Glu299Arg
ENST00000371953.7:c.895_896delinsCG	ENSP00000361021.3:p.Glu299Arg
ENST00000472832.2:c.322_323delinsCG	ENSP00000483066.1:p.Glu108Arg
NM_000314.5:c.895_896delinsCG	NP_000305.3:p.Glu299Arg
NM_000314.6:c.895_896delinsCG	NP_000305.3:p.Glu299Arg
NM_001304717.2:c.1414_1415delinsCG	NP_001291646.2:p.Glu472Arg
NM_001304718.1:c.304_305delinsCG	NP_001291647.1:p.Glu102Arg
XM_006717926.2:c.850_851delinsCG	XP_006717989.1:p.Glu284Arg
XM_011539981.1:c.895_896delinsCG	XP_011538283.1:p.Glu299Arg
XM_011539982.1:c.799_800delinsCG	XP_011538284.1:p.Glu267Arg
XR_945791.1:n.1465_1466delinsCG
NM_000314.7:c.895_896delinsCG	NP_000305.3:p.Glu299Arg
NM_001304717.5:c.1414_1415delinsCG	NP_001291646.4:p.Glu472Arg
NM_001304718.2:c.304_305delinsCG	NP_001291647.1:p.Glu102Arg
NM_000314.8:c.895_896delinsCG MANE Select	NP_000305.3:p.Glu299Arg