Canonical Allele Identifier: CA891836259

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961024_87961025delinsTG , CM000672.2:g.87961024_87961025delinsTG	GRCh38
NC_000010.10:g.89720781_89720782delinsTG , CM000672.1:g.89720781_89720782delinsTG	GRCh37
NC_000010.9:g.89710761_89710762delinsTG	NCBI36
NG_007466.2:g.102586_102587delinsTG , LRG_311:g.102586_102587delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1025_1026delinsTG	ENSP00000514759.2:p.Asn342Met
ENST00000710265.1:c.932_933delinsTG	ENSP00000518161.1:p.Asn311Met
ENST00000472832.3:c.932_933delinsTG	ENSP00000483066.2:p.Asn311Met
ENST00000688158.2:n.1667_1668delinsTG
ENST00000688922.2:c.*762_*763delinsTG	ENSP00000508742.2:n.*762_*763delinsTG
ENST00000700021.1:c.887_888delinsTG	ENSP00000514757.1:p.Asn296Met
ENST00000700022.1:c.*271_*272delinsTG	ENSP00000514758.1:n.*271_*272delinsTG
ENST00000700023.1:n.2090_2091delinsTG
ENST00000700024.1:n.2324_2325delinsTG
ENST00000700025.1:n.1701_1702delinsTG
ENST00000700026.1:n.569_570delinsTG
ENST00000706954.1:c.932_933delinsTG	ENSP00000516674.1:p.Asn311Met
ENST00000706955.1:c.*967_*968delinsTG	ENSP00000516675.1:n.*967_*968delinsTG
ENST00000686459.1:c.*518_*519delinsTG	ENSP00000508909.1:n.*518_*519delinsTG
ENST00000688158.1:c.*1043_*1044delinsTG	ENSP00000509254.1:n.*1043_*1044delinsTG
ENST00000688308.1:c.932_933delinsTG	ENSP00000508752.1:p.Asn311Met
ENST00000688922.1:c.853_854delinsTG
ENST00000693560.1:c.1451_1452delinsTG	ENSP00000509861.1:p.Asn484Met
ENST00000371953.8:c.932_933delinsTG MANE Select	ENSP00000361021.3:p.Asn311Met
ENST00000371953.7:c.932_933delinsTG	ENSP00000361021.3:p.Asn311Met
ENST00000472832.2:c.359_360delinsTG	ENSP00000483066.1:p.Asn120Met
NM_000314.5:c.932_933delinsTG	NP_000305.3:p.Asn311Met
NM_000314.6:c.932_933delinsTG	NP_000305.3:p.Asn311Met
NM_001304717.2:c.1451_1452delinsTG	NP_001291646.2:p.Asn484Met
NM_001304718.1:c.341_342delinsTG	NP_001291647.1:p.Asn114Met
XM_006717926.2:c.887_888delinsTG	XP_006717989.1:p.Asn296Met
XM_011539981.1:c.932_933delinsTG	XP_011538283.1:p.Asn311Met
XM_011539982.1:c.836_837delinsTG	XP_011538284.1:p.Asn279Met
XR_945791.1:n.1502_1503delinsTG
NM_000314.7:c.932_933delinsTG	NP_000305.3:p.Asn311Met
NM_001304717.5:c.1451_1452delinsTG	NP_001291646.4:p.Asn484Met
NM_001304718.2:c.341_342delinsTG	NP_001291647.1:p.Asn114Met
NM_000314.8:c.932_933delinsTG MANE Select	NP_000305.3:p.Asn311Met