Canonical Allele Identifier: CA470667581

Gene: PTEN

Linked Data

• COSMIC: COSM921109
• MyVariant Identifiers: chr10:g.89711896del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952139del , CM000672.2:g.87952139del	GRCh38
NC_000010.10:g.89711896del , CM000672.1:g.89711896del	GRCh37
NC_000010.9:g.89701876del	NCBI36
NG_007466.2:g.93701del , LRG_311:g.93701del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.514del	ENSP00000514759.2:p.Arg172GlyfsTer11
ENST00000710265.1:c.514del	ENSP00000518161.1:p.Arg172GlyfsTer11
ENST00000472832.3:c.514del	ENSP00000483066.2:p.Arg172GlyfsTer11
ENST00000688158.2:n.1249del
ENST00000688922.2:c.*344del	ENSP00000508742.2:n.*344del
ENST00000700021.1:c.469del	ENSP00000514757.1:p.Arg157GlyfsTer11
ENST00000700022.1:c.493-5714del	ENSP00000514758.1:n.493-5714del
ENST00000700023.1:n.1672del
ENST00000700024.1:n.1906del
ENST00000700025.1:n.1283del
ENST00000700029.1:c.348del
ENST00000706954.1:c.514del	ENSP00000516674.1:p.Arg172GlyfsTer11
ENST00000706955.1:c.*549del	ENSP00000516675.1:n.*549del
ENST00000686459.1:c.*100del	ENSP00000508909.1:n.*100del
ENST00000688158.1:c.*625del	ENSP00000509254.1:n.*625del
ENST00000688308.1:c.514del	ENSP00000508752.1:p.Arg172GlyfsTer11
ENST00000688922.1:c.435del
ENST00000693560.1:c.1033del	ENSP00000509861.1:p.Arg345GlyfsTer11
ENST00000371953.8:c.514del MANE Select	ENSP00000361021.3:p.Arg172GlyfsTer11
ENST00000371953.7:c.514del	ENSP00000361021.3:p.Arg172GlyfsTer11
NM_000314.5:c.514del	NP_000305.3:p.Arg172GlyfsTer11
NM_000314.6:c.514del	NP_000305.3:p.Arg172GlyfsTer11
NM_001304717.2:c.1033del	NP_001291646.2:p.Arg345GlyfsTer11
NM_001304718.1:c.-78del	NP_001291647.1:n.-78del
XM_006717926.2:c.469del	XP_006717989.1:p.Arg157GlyfsTer11
XM_011539981.1:c.514del	XP_011538283.1:p.Arg172GlyfsTer11
XM_011539982.1:c.418del	XP_011538284.1:p.Arg140GlyfsTer11
XR_945789.1:n.1385del
XR_945790.1:n.1502del
XR_945791.1:n.1205-5714del
NM_000314.7:c.514del	NP_000305.3:p.Arg172GlyfsTer11
NM_001304717.5:c.1033del	NP_001291646.4:p.Arg345GlyfsTer11
NM_001304718.2:c.-78del	NP_001291647.1:n.-78del
NM_000314.8:c.514del MANE Select	NP_000305.3:p.Arg172GlyfsTer11