Canonical Allele Identifier: CA2658948766

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47800792_47800812del , CM000664.2:g.47800792_47800812del GRCh38
NC_000002.11:g.48027931_48027951del , CM000664.1:g.48027931_48027951del GRCh37
NC_000002.10:g.47881435_47881455del NCBI36
NG_007111.1:g.22646_22666del , LRG_219:g.22646_22666del

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.2512_2532del (MSH6) ENSP00000406248.2:p.Tyr838_Asp844del
ENST00000420813.6:c.2512_2532del (MSH6) ENSP00000390382.2:p.Tyr838_Asp844del
ENST00000455383.6:c.2512_2532del (MSH6) ENSP00000397484.2:p.Tyr838_Asp844del
ENST00000700004.2:c.2809_2829del (MSH6) ENSP00000514752.2:p.Tyr937_Asp943del
ENST00000699999.1:n.2893_2913del (MSH6)
ENST00000700000.1:c.1606+1203_1606+1223del (MSH6) ENSP00000514749.1:n.1606+1203_1606+1223del
ENST00000700002.1:c.2815_2835del (MSH6) ENSP00000514750.1:p.Tyr939_Asp945del
ENST00000700003.1:c.628-2628_628-2608del (MSH6) ENSP00000514751.1:n.628-2628_628-2608del
ENST00000700004.1:c.1966_1986del (MSH6) ENSP00000514752.1:p.Tyr656_Asp662del
ENST00000234420.11:c.2809_2829del (MSH6) MANE Select ENSP00000234420.5:p.Tyr937_Asp943del
ENST00000540021.6:c.2419_2439del (MSH6) ENSP00000446475.1:p.Tyr807_Asp813del
ENST00000652107.1:c.2512_2532del (MSH6) ENSP00000498629.1:p.Tyr838_Asp844del
ENST00000673637.1:c.2512_2532del (MSH6) ENSP00000501310.1:p.Tyr838_Asp844del
ENST00000234420.9:c.2809_2829del (MSH6) ENSP00000234420.4:p.Tyr937_Asp943del
ENST00000405808.5:c.169+7383_169+7403del (FBXO11) ENSP00000385127.1:n.169+7383_169+7403del
ENST00000434234.5:c.*124+7182_*124+7202del (FBXO11) ENSP00000402692.1:n.*124+7182_*124+7202del
ENST00000445503.5:c.*2156_*2176del (MSH6) ENSP00000405294.1:n.*2156_*2176del
ENST00000538136.1:c.1903_1923del (MSH6) ENSP00000438580.1:p.Tyr635_Asp641del
ENST00000540021.5:c.2419_2439del (MSH6) ENSP00000446475.1:p.Tyr807_Asp813del
ENST00000614496.4:c.1903_1923del (MSH6) ENSP00000477844.1:p.Tyr635_Asp641del
ENST00000616033.4:c.2806_2826del (MSH6) ENSP00000480261.1:p.Tyr936_Asp942del
ENST00000622629.4:c.-288_-268del (MSH6) ENSP00000482078.1:n.-288_-268del
NM_000179.2:c.2809_2829del , LRG_219t1:c.2809_2829del (MSH6) NP_000170.1:p.Tyr937_Asp943del
NM_001281492.1:c.2419_2439del (MSH6) NP_001268421.1:p.Tyr807_Asp813del
NM_001281493.1:c.1903_1923del (MSH6) NP_001268422.1:p.Tyr635_Asp641del
NM_001281494.1:c.1903_1923del (MSH6) NP_001268423.1:p.Tyr635_Asp641del
XM_005264271.1:c.2512_2532del (MSH6) XP_005264328.1:p.Tyr838_Asp844del
XM_011532798.1:c.2626_2646del (MSH6) XP_011531100.1:p.Tyr876_Asp882del
XM_011532799.1:c.2512_2532del (MSH6) XP_011531101.1:p.Tyr838_Asp844del
XM_011532800.1:c.2512_2532del (MSH6) XP_011531102.1:p.Tyr838_Asp844del
XM_024452819.1:c.2809_2829del (MSH6) XP_024308587.1:p.Tyr937_Asp943del
XM_024452820.1:c.2626_2646del (MSH6) XP_024308588.1:p.Tyr876_Asp882del
XM_024452821.1:c.2512_2532del (MSH6) XP_024308589.1:p.Tyr838_Asp844del
XM_024452822.1:c.1903_1923del (MSH6) XP_024308590.1:p.Tyr635_Asp641del
NM_000179.3:c.2809_2829del (MSH6) MANE Select NP_000170.1:p.Tyr937_Asp943del
NM_001281492.2:c.2419_2439del (MSH6) NP_001268421.1:p.Tyr807_Asp813del
NM_001281493.2:c.1903_1923del (MSH6) NP_001268422.1:p.Tyr635_Asp641del
NM_001281494.2:c.1903_1923del (MSH6) NP_001268423.1:p.Tyr635_Asp641del