Canonical Allele Identifier: CA891836682

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961059_87961060delinsGC , CM000672.2:g.87961059_87961060delinsGC	GRCh38
NC_000010.10:g.89720816_89720817delinsGC , CM000672.1:g.89720816_89720817delinsGC	GRCh37
NC_000010.9:g.89710796_89710797delinsGC	NCBI36
NG_007466.2:g.102621_102622delinsGC , LRG_311:g.102621_102622delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1060_1061delinsGC	ENSP00000514759.2:p.Asn354Ala
ENST00000710265.1:c.967_968delinsGC	ENSP00000518161.1:p.Asn323Ala
ENST00000472832.3:c.967_968delinsGC	ENSP00000483066.2:p.Asn323Ala
ENST00000688158.2:n.1702_1703delinsGC
ENST00000688922.2:c.*797_*798delinsGC	ENSP00000508742.2:n.*797_*798delinsGC
ENST00000700021.1:c.922_923delinsGC	ENSP00000514757.1:p.Asn308Ala
ENST00000700022.1:c.*306_*307delinsGC	ENSP00000514758.1:n.*306_*307delinsGC
ENST00000700023.1:n.2125_2126delinsGC
ENST00000700024.1:n.2359_2360delinsGC
ENST00000700025.1:n.1736_1737delinsGC
ENST00000700026.1:n.604_605delinsGC
ENST00000706954.1:c.967_968delinsGC	ENSP00000516674.1:p.Asn323Ala
ENST00000706955.1:c.*1002_*1003delinsGC	ENSP00000516675.1:n.*1002_*1003delinsGC
ENST00000686459.1:c.*553_*554delinsGC	ENSP00000508909.1:n.*553_*554delinsGC
ENST00000688158.1:c.*1078_*1079delinsGC	ENSP00000509254.1:n.*1078_*1079delinsGC
ENST00000688308.1:c.967_968delinsGC	ENSP00000508752.1:p.Asn323Ala
ENST00000688922.1:c.888_889delinsGC
ENST00000693560.1:c.1486_1487delinsGC	ENSP00000509861.1:p.Asn496Ala
ENST00000371953.8:c.967_968delinsGC MANE Select	ENSP00000361021.3:p.Asn323Ala
ENST00000371953.7:c.967_968delinsGC	ENSP00000361021.3:p.Asn323Ala
ENST00000472832.2:c.394_395delinsGC	ENSP00000483066.1:p.Asn132Ala
NM_000314.5:c.967_968delinsGC	NP_000305.3:p.Asn323Ala
NM_000314.6:c.967_968delinsGC	NP_000305.3:p.Asn323Ala
NM_001304717.2:c.1486_1487delinsGC	NP_001291646.2:p.Asn496Ala
NM_001304718.1:c.376_377delinsGC	NP_001291647.1:p.Asn126Ala
XM_006717926.2:c.922_923delinsGC	XP_006717989.1:p.Asn308Ala
XM_011539981.1:c.967_968delinsGC	XP_011538283.1:p.Asn323Ala
XM_011539982.1:c.871_872delinsGC	XP_011538284.1:p.Asn291Ala
XR_945791.1:n.1537_1538delinsGC
NM_000314.7:c.967_968delinsGC	NP_000305.3:p.Asn323Ala
NM_001304717.5:c.1486_1487delinsGC	NP_001291646.4:p.Asn496Ala
NM_001304718.2:c.376_377delinsGC	NP_001291647.1:p.Asn126Ala
NM_000314.8:c.967_968delinsGC MANE Select	NP_000305.3:p.Asn323Ala