Canonical Allele Identifier: CA645554071

Gene: PTEN

Linked Data

• COSMIC: COSM1173632

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87958012_87958013insG , CM000672.2:g.87958012_87958013insG	GRCh38
NC_000010.10:g.89717769_89717770insG , CM000672.1:g.89717769_89717770insG	GRCh37
NC_000010.9:g.89707749_89707750insG	NCBI36
NG_007466.2:g.99574_99575insG , LRG_311:g.99574_99575insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.794_795insG	ENSP00000514759.2:p.Gln269ThrfsTer?
ENST00000710265.1:c.794_795insG	ENSP00000518161.1:p.Asp268GlyfsTer?
ENST00000472832.3:c.794_795insG	ENSP00000483066.2:p.Asp268GlyfsTer?
ENST00000688158.2:n.1529_1530insG
ENST00000688922.2:c.*624_*625insG	ENSP00000508742.2:n.*624_*625insG
ENST00000700021.1:c.749_750insG	ENSP00000514757.1:p.Asp253GlyfsTer?
ENST00000700022.1:c.*133_*134insG	ENSP00000514758.1:n.*133_*134insG
ENST00000700023.1:n.1952_1953insG
ENST00000700024.1:n.2186_2187insG
ENST00000700025.1:n.1563_1564insG
ENST00000700026.1:n.431_432insG
ENST00000700029.1:c.628_629insG
ENST00000706954.1:c.794_795insG	ENSP00000516674.1:p.Asp268GlyfsTer?
ENST00000706955.1:c.*829_*830insG	ENSP00000516675.1:n.*829_*830insG
ENST00000686459.1:c.*380_*381insG	ENSP00000508909.1:n.*380_*381insG
ENST00000688158.1:c.*905_*906insG	ENSP00000509254.1:n.*905_*906insG
ENST00000688308.1:c.794_795insG	ENSP00000508752.1:p.Asp268GlyfsTer?
ENST00000688922.1:c.715_716insG
ENST00000693560.1:c.1313_1314insG	ENSP00000509861.1:p.Asp441GlyfsTer?
ENST00000371953.8:c.794_795insG MANE Select	ENSP00000361021.3:p.Asp268GlyfsTer?
ENST00000371953.7:c.794_795insG	ENSP00000361021.3:p.Asp268GlyfsTer?
ENST00000472832.2:c.221_222insG	ENSP00000483066.1:p.Asp77GlyfsTer?
NM_000314.5:c.794_795insG	NP_000305.3:p.Asp268GlyfsTer?
NM_000314.6:c.794_795insG	NP_000305.3:p.Asp268GlyfsTer?
NM_001304717.2:c.1313_1314insG	NP_001291646.2:p.Asp441GlyfsTer?
NM_001304718.1:c.203_204insG	NP_001291647.1:p.Asp71GlyfsTer?
XM_006717926.2:c.749_750insG	XP_006717989.1:p.Asp253GlyfsTer?
XM_011539981.1:c.794_795insG	XP_011538283.1:p.Asp268GlyfsTer?
XM_011539982.1:c.698_699insG	XP_011538284.1:p.Asp236GlyfsTer?
XR_945791.1:n.1364_1365insG
NM_000314.7:c.794_795insG	NP_000305.3:p.Asp268GlyfsTer?
NM_001304717.5:c.1313_1314insG	NP_001291646.4:p.Asp441GlyfsTer?
NM_001304718.2:c.203_204insG	NP_001291647.1:p.Asp71GlyfsTer?
NM_000314.8:c.794_795insG MANE Select	NP_000305.3:p.Asp268GlyfsTer?