Canonical Allele Identifier: CA891835274

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960966_87960968delinsTGG , CM000672.2:g.87960966_87960968delinsTGG	GRCh38
NC_000010.10:g.89720723_89720725delinsTGG , CM000672.1:g.89720723_89720725delinsTGG	GRCh37
NC_000010.9:g.89710703_89710705delinsTGG	NCBI36
NG_007466.2:g.102528_102530delinsTGG , LRG_311:g.102528_102530delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.967_969delinsTGG	ENSP00000514759.2:p.Asn323Trp
ENST00000710265.1:c.874_876delinsTGG	ENSP00000518161.1:p.Asn292Trp
ENST00000472832.3:c.874_876delinsTGG	ENSP00000483066.2:p.Asn292Trp
ENST00000688158.2:n.1609_1611delinsTGG
ENST00000688922.2:c.*704_*706delinsTGG	ENSP00000508742.2:n.*704_*706delinsTGG
ENST00000700021.1:c.829_831delinsTGG	ENSP00000514757.1:p.Asn277Trp
ENST00000700022.1:c.*213_*215delinsTGG	ENSP00000514758.1:n.*213_*215delinsTGG
ENST00000700023.1:n.2032_2034delinsTGG
ENST00000700024.1:n.2266_2268delinsTGG
ENST00000700025.1:n.1643_1645delinsTGG
ENST00000700026.1:n.511_513delinsTGG
ENST00000700029.1:c.801_803delinsTGG
ENST00000706954.1:c.874_876delinsTGG	ENSP00000516674.1:p.Asn292Trp
ENST00000706955.1:c.*909_*911delinsTGG	ENSP00000516675.1:n.*909_*911delinsTGG
ENST00000686459.1:c.*460_*462delinsTGG	ENSP00000508909.1:n.*460_*462delinsTGG
ENST00000688158.1:c.*985_*987delinsTGG	ENSP00000509254.1:n.*985_*987delinsTGG
ENST00000688308.1:c.874_876delinsTGG	ENSP00000508752.1:p.Asn292Trp
ENST00000688922.1:c.795_797delinsTGG
ENST00000693560.1:c.1393_1395delinsTGG	ENSP00000509861.1:p.Asn465Trp
ENST00000371953.8:c.874_876delinsTGG MANE Select	ENSP00000361021.3:p.Asn292Trp
ENST00000371953.7:c.874_876delinsTGG	ENSP00000361021.3:p.Asn292Trp
ENST00000472832.2:c.301_303delinsTGG	ENSP00000483066.1:p.Asn101Trp
NM_000314.5:c.874_876delinsTGG	NP_000305.3:p.Asn292Trp
NM_000314.6:c.874_876delinsTGG	NP_000305.3:p.Asn292Trp
NM_001304717.2:c.1393_1395delinsTGG	NP_001291646.2:p.Asn465Trp
NM_001304718.1:c.283_285delinsTGG	NP_001291647.1:p.Asn95Trp
XM_006717926.2:c.829_831delinsTGG	XP_006717989.1:p.Asn277Trp
XM_011539981.1:c.874_876delinsTGG	XP_011538283.1:p.Asn292Trp
XM_011539982.1:c.778_780delinsTGG	XP_011538284.1:p.Asn260Trp
XR_945791.1:n.1444_1446delinsTGG
NM_000314.7:c.874_876delinsTGG	NP_000305.3:p.Asn292Trp
NM_001304717.5:c.1393_1395delinsTGG	NP_001291646.4:p.Asn465Trp
NM_001304718.2:c.283_285delinsTGG	NP_001291647.1:p.Asn95Trp
NM_000314.8:c.874_876delinsTGG MANE Select	NP_000305.3:p.Asn292Trp