Canonical Allele Identifier: CA891841117

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960966_87960967delinsCG , CM000672.2:g.87960966_87960967delinsCG	GRCh38
NC_000010.10:g.89720723_89720724delinsCG , CM000672.1:g.89720723_89720724delinsCG	GRCh37
NC_000010.9:g.89710703_89710704delinsCG	NCBI36
NG_007466.2:g.102528_102529delinsCG , LRG_311:g.102528_102529delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.967_968delinsCG	ENSP00000514759.2:p.Asn323Arg
ENST00000710265.1:c.874_875delinsCG	ENSP00000518161.1:p.Asn292Arg
ENST00000472832.3:c.874_875delinsCG	ENSP00000483066.2:p.Asn292Arg
ENST00000688158.2:n.1609_1610delinsCG
ENST00000688922.2:c.*704_*705delinsCG	ENSP00000508742.2:n.*704_*705delinsCG
ENST00000700021.1:c.829_830delinsCG	ENSP00000514757.1:p.Asn277Arg
ENST00000700022.1:c.*213_*214delinsCG	ENSP00000514758.1:n.*213_*214delinsCG
ENST00000700023.1:n.2032_2033delinsCG
ENST00000700024.1:n.2266_2267delinsCG
ENST00000700025.1:n.1643_1644delinsCG
ENST00000700026.1:n.511_512delinsCG
ENST00000700029.1:c.801_802delinsCG
ENST00000706954.1:c.874_875delinsCG	ENSP00000516674.1:p.Asn292Arg
ENST00000706955.1:c.*909_*910delinsCG	ENSP00000516675.1:n.*909_*910delinsCG
ENST00000686459.1:c.*460_*461delinsCG	ENSP00000508909.1:n.*460_*461delinsCG
ENST00000688158.1:c.*985_*986delinsCG	ENSP00000509254.1:n.*985_*986delinsCG
ENST00000688308.1:c.874_875delinsCG	ENSP00000508752.1:p.Asn292Arg
ENST00000688922.1:c.795_796delinsCG
ENST00000693560.1:c.1393_1394delinsCG	ENSP00000509861.1:p.Asn465Arg
ENST00000371953.8:c.874_875delinsCG MANE Select	ENSP00000361021.3:p.Asn292Arg
ENST00000371953.7:c.874_875delinsCG	ENSP00000361021.3:p.Asn292Arg
ENST00000472832.2:c.301_302delinsCG	ENSP00000483066.1:p.Asn101Arg
NM_000314.5:c.874_875delinsCG	NP_000305.3:p.Asn292Arg
NM_000314.6:c.874_875delinsCG	NP_000305.3:p.Asn292Arg
NM_001304717.2:c.1393_1394delinsCG	NP_001291646.2:p.Asn465Arg
NM_001304718.1:c.283_284delinsCG	NP_001291647.1:p.Asn95Arg
XM_006717926.2:c.829_830delinsCG	XP_006717989.1:p.Asn277Arg
XM_011539981.1:c.874_875delinsCG	XP_011538283.1:p.Asn292Arg
XM_011539982.1:c.778_779delinsCG	XP_011538284.1:p.Asn260Arg
XR_945791.1:n.1444_1445delinsCG
NM_000314.7:c.874_875delinsCG	NP_000305.3:p.Asn292Arg
NM_001304717.5:c.1393_1394delinsCG	NP_001291646.4:p.Asn465Arg
NM_001304718.2:c.283_284delinsCG	NP_001291647.1:p.Asn95Arg
NM_000314.8:c.874_875delinsCG MANE Select	NP_000305.3:p.Asn292Arg