Canonical Allele Identifier: CA891840273

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960919_87960920delinsGA , CM000672.2:g.87960919_87960920delinsGA	GRCh38
NC_000010.10:g.89720676_89720677delinsGA , CM000672.1:g.89720676_89720677delinsGA	GRCh37
NC_000010.9:g.89710656_89710657delinsGA	NCBI36
NG_007466.2:g.102481_102482delinsGA , LRG_311:g.102481_102482delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.920_921delinsGA	ENSP00000514759.2:p.Asn307Arg
ENST00000710265.1:c.827_828delinsGA	ENSP00000518161.1:p.Asn276Arg
ENST00000472832.3:c.827_828delinsGA	ENSP00000483066.2:p.Asn276Arg
ENST00000688158.2:n.1562_1563delinsGA
ENST00000688922.2:c.*657_*658delinsGA	ENSP00000508742.2:n.*657_*658delinsGA
ENST00000700021.1:c.782_783delinsGA	ENSP00000514757.1:p.Asn261Arg
ENST00000700022.1:c.*166_*167delinsGA	ENSP00000514758.1:n.*166_*167delinsGA
ENST00000700023.1:n.1985_1986delinsGA
ENST00000700024.1:n.2219_2220delinsGA
ENST00000700025.1:n.1596_1597delinsGA
ENST00000700026.1:n.464_465delinsGA
ENST00000700029.1:c.754_755delinsGA
ENST00000706954.1:c.827_828delinsGA	ENSP00000516674.1:p.Asn276Arg
ENST00000706955.1:c.*862_*863delinsGA	ENSP00000516675.1:n.*862_*863delinsGA
ENST00000686459.1:c.*413_*414delinsGA	ENSP00000508909.1:n.*413_*414delinsGA
ENST00000688158.1:c.*938_*939delinsGA	ENSP00000509254.1:n.*938_*939delinsGA
ENST00000688308.1:c.827_828delinsGA	ENSP00000508752.1:p.Asn276Arg
ENST00000688922.1:c.748_749delinsGA
ENST00000693560.1:c.1346_1347delinsGA	ENSP00000509861.1:p.Asn449Arg
ENST00000371953.8:c.827_828delinsGA MANE Select	ENSP00000361021.3:p.Asn276Arg
ENST00000371953.7:c.827_828delinsGA	ENSP00000361021.3:p.Asn276Arg
ENST00000472832.2:c.254_255delinsGA	ENSP00000483066.1:p.Asn85Arg
NM_000314.5:c.827_828delinsGA	NP_000305.3:p.Asn276Arg
NM_000314.6:c.827_828delinsGA	NP_000305.3:p.Asn276Arg
NM_001304717.2:c.1346_1347delinsGA	NP_001291646.2:p.Asn449Arg
NM_001304718.1:c.236_237delinsGA	NP_001291647.1:p.Asn79Arg
XM_006717926.2:c.782_783delinsGA	XP_006717989.1:p.Asn261Arg
XM_011539981.1:c.827_828delinsGA	XP_011538283.1:p.Asn276Arg
XM_011539982.1:c.731_732delinsGA	XP_011538284.1:p.Asn244Arg
XR_945791.1:n.1397_1398delinsGA
NM_000314.7:c.827_828delinsGA	NP_000305.3:p.Asn276Arg
NM_001304717.5:c.1346_1347delinsGA	NP_001291646.4:p.Asn449Arg
NM_001304718.2:c.236_237delinsGA	NP_001291647.1:p.Asn79Arg
NM_000314.8:c.827_828delinsGA MANE Select	NP_000305.3:p.Asn276Arg