Canonical Allele Identifier: CA891835271

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960966_87960967delinsTG , CM000672.2:g.87960966_87960967delinsTG	GRCh38
NC_000010.10:g.89720723_89720724delinsTG , CM000672.1:g.89720723_89720724delinsTG	GRCh37
NC_000010.9:g.89710703_89710704delinsTG	NCBI36
NG_007466.2:g.102528_102529delinsTG , LRG_311:g.102528_102529delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.967_968delinsTG	ENSP00000514759.2:p.Asn323Cys
ENST00000710265.1:c.874_875delinsTG	ENSP00000518161.1:p.Asn292Cys
ENST00000472832.3:c.874_875delinsTG	ENSP00000483066.2:p.Asn292Cys
ENST00000688158.2:n.1609_1610delinsTG
ENST00000688922.2:c.*704_*705delinsTG	ENSP00000508742.2:n.*704_*705delinsTG
ENST00000700021.1:c.829_830delinsTG	ENSP00000514757.1:p.Asn277Cys
ENST00000700022.1:c.*213_*214delinsTG	ENSP00000514758.1:n.*213_*214delinsTG
ENST00000700023.1:n.2032_2033delinsTG
ENST00000700024.1:n.2266_2267delinsTG
ENST00000700025.1:n.1643_1644delinsTG
ENST00000700026.1:n.511_512delinsTG
ENST00000700029.1:c.801_802delinsTG
ENST00000706954.1:c.874_875delinsTG	ENSP00000516674.1:p.Asn292Cys
ENST00000706955.1:c.*909_*910delinsTG	ENSP00000516675.1:n.*909_*910delinsTG
ENST00000686459.1:c.*460_*461delinsTG	ENSP00000508909.1:n.*460_*461delinsTG
ENST00000688158.1:c.*985_*986delinsTG	ENSP00000509254.1:n.*985_*986delinsTG
ENST00000688308.1:c.874_875delinsTG	ENSP00000508752.1:p.Asn292Cys
ENST00000688922.1:c.795_796delinsTG
ENST00000693560.1:c.1393_1394delinsTG	ENSP00000509861.1:p.Asn465Cys
ENST00000371953.8:c.874_875delinsTG MANE Select	ENSP00000361021.3:p.Asn292Cys
ENST00000371953.7:c.874_875delinsTG	ENSP00000361021.3:p.Asn292Cys
ENST00000472832.2:c.301_302delinsTG	ENSP00000483066.1:p.Asn101Cys
NM_000314.5:c.874_875delinsTG	NP_000305.3:p.Asn292Cys
NM_000314.6:c.874_875delinsTG	NP_000305.3:p.Asn292Cys
NM_001304717.2:c.1393_1394delinsTG	NP_001291646.2:p.Asn465Cys
NM_001304718.1:c.283_284delinsTG	NP_001291647.1:p.Asn95Cys
XM_006717926.2:c.829_830delinsTG	XP_006717989.1:p.Asn277Cys
XM_011539981.1:c.874_875delinsTG	XP_011538283.1:p.Asn292Cys
XM_011539982.1:c.778_779delinsTG	XP_011538284.1:p.Asn260Cys
XR_945791.1:n.1444_1445delinsTG
NM_000314.7:c.874_875delinsTG	NP_000305.3:p.Asn292Cys
NM_001304717.5:c.1393_1394delinsTG	NP_001291646.4:p.Asn465Cys
NM_001304718.2:c.283_284delinsTG	NP_001291647.1:p.Asn95Cys
NM_000314.8:c.874_875delinsTG MANE Select	NP_000305.3:p.Asn292Cys