Canonical Allele Identifier: CA891836847

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961078_87961079delinsGA , CM000672.2:g.87961078_87961079delinsGA	GRCh38
NC_000010.10:g.89720835_89720836delinsGA , CM000672.1:g.89720835_89720836delinsGA	GRCh37
NC_000010.9:g.89710815_89710816delinsGA	NCBI36
NG_007466.2:g.102640_102641delinsGA , LRG_311:g.102640_102641delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1079_1080delinsGA	ENSP00000514759.2:p.Asn360Arg
ENST00000710265.1:c.986_987delinsGA	ENSP00000518161.1:p.Asn329Arg
ENST00000472832.3:c.986_987delinsGA	ENSP00000483066.2:p.Asn329Arg
ENST00000688158.2:n.1721_1722delinsGA
ENST00000688922.2:c.*816_*817delinsGA	ENSP00000508742.2:n.*816_*817delinsGA
ENST00000700021.1:c.941_942delinsGA	ENSP00000514757.1:p.Asn314Arg
ENST00000700022.1:c.*325_*326delinsGA	ENSP00000514758.1:n.*325_*326delinsGA
ENST00000700023.1:n.2144_2145delinsGA
ENST00000700024.1:n.2378_2379delinsGA
ENST00000700025.1:n.1755_1756delinsGA
ENST00000700026.1:n.623_624delinsGA
ENST00000706954.1:c.986_987delinsGA	ENSP00000516674.1:p.Asn329Arg
ENST00000706955.1:c.*1021_*1022delinsGA	ENSP00000516675.1:n.*1021_*1022delinsGA
ENST00000686459.1:c.*572_*573delinsGA	ENSP00000508909.1:n.*572_*573delinsGA
ENST00000688158.1:c.*1097_*1098delinsGA	ENSP00000509254.1:n.*1097_*1098delinsGA
ENST00000688308.1:c.986_987delinsGA	ENSP00000508752.1:p.Asn329Arg
ENST00000688922.1:c.907_908delinsGA
ENST00000693560.1:c.1505_1506delinsGA	ENSP00000509861.1:p.Asn502Arg
ENST00000371953.8:c.986_987delinsGA MANE Select	ENSP00000361021.3:p.Asn329Arg
ENST00000371953.7:c.986_987delinsGA	ENSP00000361021.3:p.Asn329Arg
ENST00000472832.2:c.413_414delinsGA	ENSP00000483066.1:p.Asn138Arg
NM_000314.5:c.986_987delinsGA	NP_000305.3:p.Asn329Arg
NM_000314.6:c.986_987delinsGA	NP_000305.3:p.Asn329Arg
NM_001304717.2:c.1505_1506delinsGA	NP_001291646.2:p.Asn502Arg
NM_001304718.1:c.395_396delinsGA	NP_001291647.1:p.Asn132Arg
XM_006717926.2:c.941_942delinsGA	XP_006717989.1:p.Asn314Arg
XM_011539981.1:c.986_987delinsGA	XP_011538283.1:p.Asn329Arg
XM_011539982.1:c.890_891delinsGA	XP_011538284.1:p.Asn297Arg
XR_945791.1:n.1556_1557delinsGA
NM_000314.7:c.986_987delinsGA	NP_000305.3:p.Asn329Arg
NM_001304717.5:c.1505_1506delinsGA	NP_001291646.4:p.Asn502Arg
NM_001304718.2:c.395_396delinsGA	NP_001291647.1:p.Asn132Arg
NM_000314.8:c.986_987delinsGA MANE Select	NP_000305.3:p.Asn329Arg