Canonical Allele Identifier: CA2695200574

Linked Data

ClinVar Variation Id: 2673702
ClinVar RCV Id: RCV003450339

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47799409_47799410insGGGCCGTTATTCAGATTCCCTGGTGCAGA , CM000664.2:g.47799409_47799410insGGGCCGTTATTCAGATTCCCTGGTGCAGA GRCh38
NC_000002.11:g.48026548_48026549insGGGCCGTTATTCAGATTCCCTGGTGCAGA , CM000664.1:g.48026548_48026549insGGGCCGTTATTCAGATTCCCTGGTGCAGA GRCh37
NC_000002.10:g.47880052_47880053insGGGCCGTTATTCAGATTCCCTGGTGCAGA NCBI36
NG_007111.1:g.21263_21264insGGGCCGTTATTCAGATTCCCTGGTGCAGA , LRG_219:g.21263_21264insGGGCCGTTATTCAGATTCCCTGGTGCAGA

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.1129_1130insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) ENSP00000406248.2:p.Lys377ArgfsTer15
ENST00000420813.6:c.1129_1130insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) ENSP00000390382.2:p.Lys377ArgfsTer15
ENST00000455383.6:c.1129_1130insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) ENSP00000397484.2:p.Lys377ArgfsTer15
ENST00000700004.2:c.1426_1427insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) ENSP00000514752.2:p.Lys476ArgfsTer15
ENST00000699999.1:n.1510_1511insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6)
ENST00000700000.1:c.1426_1427insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) ENSP00000514749.1:p.Lys476ArgfsTer15
ENST00000700002.1:c.1432_1433insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) ENSP00000514750.1:p.Lys478ArgfsTer15
ENST00000700003.1:c.627+3346_627+3347insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) ENSP00000514751.1:n.627+3346_627+3347insG...
ENST00000700004.1:c.583_584insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) ENSP00000514752.1:p.Lys195ArgfsTer15
ENST00000234420.11:c.1426_1427insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) MANE Select ENSP00000234420.5:p.Lys476ArgfsTer15
ENST00000540021.6:c.1036_1037insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) ENSP00000446475.1:p.Lys346ArgfsTer15
ENST00000652107.1:c.1129_1130insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) ENSP00000498629.1:p.Lys377ArgfsTer15
ENST00000673637.1:c.1129_1130insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) ENSP00000501310.1:p.Lys377ArgfsTer15
ENST00000234420.9:c.1426_1427insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) ENSP00000234420.4:p.Lys476ArgfsTer15
ENST00000405808.5:c.169+8813_169+8814insCTCTGCACCAGGGAATCTGAATAACGGCC (FBXO11) ENSP00000385127.1:n.169+8813_169+8814insC...
ENST00000434234.5:c.*124+8612_*124+8613insCTCTGCACCAGGGAATCTGAATAACGGCC (FBXO11) ENSP00000402692.1:n.*124+8612_*124+8613in...
ENST00000445503.5:c.*773_*774insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) ENSP00000405294.1:n.*773_*774insGGGCCGTTA...
ENST00000538136.1:c.520_521insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) ENSP00000438580.1:p.Lys174ArgfsTer15
ENST00000540021.5:c.1036_1037insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) ENSP00000446475.1:p.Lys346ArgfsTer15
ENST00000614496.4:c.520_521insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) ENSP00000477844.1:p.Lys174ArgfsTer15
ENST00000616033.4:c.1423_1424insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) ENSP00000480261.1:p.Lys475ArgfsTer15
ENST00000622629.4:c.-1671_-1670insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) ENSP00000482078.1:n.-1671_-1670insGGGCCGT...
NM_000179.2:c.1426_1427insGGGCCGTTATTCAGATTCCCTGGTGCAGA , LRG_219t1:c.1426_1427insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) NP_000170.1:p.Lys476ArgfsTer15
NM_001281492.1:c.1036_1037insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) NP_001268421.1:p.Lys346ArgfsTer15
NM_001281493.1:c.520_521insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) NP_001268422.1:p.Lys174ArgfsTer15
NM_001281494.1:c.520_521insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) NP_001268423.1:p.Lys174ArgfsTer15
XM_005264271.1:c.1129_1130insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) XP_005264328.1:p.Lys377ArgfsTer15
XM_011532798.1:c.1243_1244insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) XP_011531100.1:p.Lys415ArgfsTer15
XM_011532799.1:c.1129_1130insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) XP_011531101.1:p.Lys377ArgfsTer15
XM_011532800.1:c.1129_1130insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) XP_011531102.1:p.Lys377ArgfsTer15
XM_024452819.1:c.1426_1427insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) XP_024308587.1:p.Lys476ArgfsTer15
XM_024452820.1:c.1243_1244insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) XP_024308588.1:p.Lys415ArgfsTer15
XM_024452821.1:c.1129_1130insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) XP_024308589.1:p.Lys377ArgfsTer15
XM_024452822.1:c.520_521insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) XP_024308590.1:p.Lys174ArgfsTer15
NM_000179.3:c.1426_1427insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) MANE Select NP_000170.1:p.Lys476ArgfsTer15
NM_001281492.2:c.1036_1037insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) NP_001268421.1:p.Lys346ArgfsTer15
NM_001281493.2:c.520_521insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) NP_001268422.1:p.Lys174ArgfsTer15
NM_001281494.2:c.520_521insGGGCCGTTATTCAGATTCCCTGGTGCAGA (MSH6) NP_001268423.1:p.Lys174ArgfsTer15