Canonical Allele Identifier: CA010436
Community Standard Title: NM_000179.3(MSH6):c.2569_2572del (p.Asp857PhefsTer10)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47800552_47800555del , CM000664.2:g.47800552_47800555del GRCh38
NC_000002.11:g.48027691_48027694del , CM000664.1:g.48027691_48027694del GRCh37
NC_000002.10:g.47881195_47881198del NCBI36
NG_007111.1:g.22406_22409del , LRG_219:g.22406_22409del

Transcript Alleles

HGVS Amino-acid Change
NM_000179.3:c.2569_2572del (MSH6) MANE Select NP_000170.1:p.Asp857PhefsTer10
ENST00000234420.11:c.2569_2572del (MSH6) MANE Select ENSP00000234420.5:p.Asp857PhefsTer10
NM_000179.2:c.2569_2572del , LRG_219t1:c.2569_2572del (MSH6) NP_000170.1:p.Asp857PhefsTer10
NM_001281492.1:c.2179_2182del (MSH6) NP_001268421.1:p.Asp727PhefsTer10
NM_001281492.2:c.2179_2182del (MSH6) NP_001268421.1:p.Asp727PhefsTer10
NM_001281493.1:c.1663_1666del (MSH6) NP_001268422.1:p.Asp555PhefsTer10
NM_001281493.2:c.1663_1666del (MSH6) NP_001268422.1:p.Asp555PhefsTer10
NM_001281494.1:c.1663_1666del (MSH6) NP_001268423.1:p.Asp555PhefsTer10
NM_001281494.2:c.1663_1666del (MSH6) NP_001268423.1:p.Asp555PhefsTer10
ENST00000234420.9:c.2569_2572del (MSH6) ENSP00000234420.4:p.Asp857PhefsTer10
ENST00000405808.5:c.169+7643_169+7646del (FBXO11) ENSP00000385127.1:n.169+7643_169+7646del
ENST00000411819.2:c.2272_2275del (MSH6) ENSP00000406248.2:p.Asp758PhefsTer10
ENST00000420813.6:c.2272_2275del (MSH6) ENSP00000390382.2:p.Asp758PhefsTer10
ENST00000434234.5:c.*124+7442_*124+7445del (FBXO11) ENSP00000402692.1:n.*124+7442_*124+7445del
ENST00000445503.5:c.*1916_*1919del (MSH6) ENSP00000405294.1:n.*1916_*1919del
ENST00000455383.6:c.2272_2275del (MSH6) ENSP00000397484.2:p.Asp758PhefsTer10
ENST00000538136.1:c.1663_1666del (MSH6) ENSP00000438580.1:p.Asp555PhefsTer10
ENST00000540021.5:c.2179_2182del (MSH6) ENSP00000446475.1:p.Asp727PhefsTer10
ENST00000540021.6:c.2179_2182del (MSH6) ENSP00000446475.1:p.Asp727PhefsTer10
ENST00000614496.4:c.1663_1666del (MSH6) ENSP00000477844.1:p.Asp555PhefsTer10
ENST00000616033.4:c.2566_2569del (MSH6) ENSP00000480261.1:p.Asp856PhefsTer10
ENST00000622629.4:c.-528_-525del (MSH6) ENSP00000482078.1:n.-528_-525del
ENST00000652107.1:c.2272_2275del (MSH6) ENSP00000498629.1:p.Asp758PhefsTer10
ENST00000673637.1:c.2272_2275del (MSH6) ENSP00000501310.1:p.Asp758PhefsTer10
ENST00000699999.1:n.2653_2656del (MSH6)
ENST00000700000.1:c.1606+963_1606+966del (MSH6) ENSP00000514749.1:n.1606+963_1606+966del
ENST00000700002.1:c.2575_2578del (MSH6) ENSP00000514750.1:p.Asp859PhefsTer10
ENST00000700003.1:c.628-2868_628-2865del (MSH6) ENSP00000514751.1:n.628-2868_628-2865del
ENST00000700004.1:c.1726_1729del (MSH6) ENSP00000514752.1:p.Asp576PhefsTer10
ENST00000700004.2:c.2569_2572del (MSH6) ENSP00000514752.2:p.Asp857PhefsTer10
XM_005264271.1:c.2272_2275del (MSH6) XP_005264328.1:p.Asp758PhefsTer10
XM_011532798.1:c.2386_2389del (MSH6) XP_011531100.1:p.Asp796PhefsTer10
XM_011532799.1:c.2272_2275del (MSH6) XP_011531101.1:p.Asp758PhefsTer10
XM_011532800.1:c.2272_2275del (MSH6) XP_011531102.1:p.Asp758PhefsTer10
XM_024452819.1:c.2569_2572del (MSH6) XP_024308587.1:p.Asp857PhefsTer10
XM_024452820.1:c.2386_2389del (MSH6) XP_024308588.1:p.Asp796PhefsTer10
XM_024452821.1:c.2272_2275del (MSH6) XP_024308589.1:p.Asp758PhefsTer10
XM_024452822.1:c.1663_1666del (MSH6) XP_024308590.1:p.Asp555PhefsTer10