Canonical Allele Identifier: CA2496053483

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47805640A= , CM000664.2:g.47805640A= GRCh38
NC_000002.11:g.48032779A= , CM000664.1:g.48032779A= GRCh37
NC_000002.10:g.47886283A= NCBI36
NG_007111.1:g.27494A= , LRG_219:g.27494A=
NG_008397.1:g.105036T=

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.3282A= (MSH6) ENSP00000406248.2:p.Glu1094=
ENST00000420813.6:c.3282A= (MSH6) ENSP00000390382.2:p.Glu1094=
ENST00000455383.6:c.3282A= (MSH6) ENSP00000397484.2:p.Glu1094=
ENST00000700004.2:c.3195A= (MSH6) ENSP00000514752.2:p.Glu1065=
ENST00000699999.1:n.4253A= (MSH6)
ENST00000700000.1:c.2013A= (MSH6) ENSP00000514749.1:p.Glu671=
ENST00000700002.1:c.3585A= (MSH6) ENSP00000514750.1:p.Glu1195=
ENST00000700003.1:c.1034A= (MSH6) ENSP00000514751.1:n.1034A=
ENST00000700004.1:c.2352A= (MSH6) ENSP00000514752.1:p.Glu784=
ENST00000700005.1:n.2430A= (MSH6)
ENST00000700006.1:n.4241A= (MSH6)
ENST00000700007.1:n.2174A= (MSH6)
ENST00000700008.1:n.1748A= (MSH6)
ENST00000700009.1:n.1747A= (MSH6)
ENST00000700010.1:n.988A= (MSH6)
ENST00000700011.1:n.2873A= (MSH6)
ENST00000234420.11:c.3579A= (MSH6) MANE Select ENSP00000234420.5:p.Glu1193=
ENST00000540021.6:c.3189A= (MSH6) ENSP00000446475.1:p.Glu1063=
ENST00000652107.1:c.3282A= (MSH6) ENSP00000498629.1:p.Glu1094=
ENST00000673637.1:c.3282A= (MSH6) ENSP00000501310.1:p.Glu1094=
ENST00000234420.9:c.3579A= (MSH6) ENSP00000234420.4:p.Glu1193=
ENST00000405808.5:c.169+2555T= (FBXO11) ENSP00000385127.1:n.169+2555T=
ENST00000434234.5:c.*124+2354T= (FBXO11) ENSP00000402692.1:n.*124+2354T=
ENST00000445503.5:c.*2926A= (MSH6) ENSP00000405294.1:n.*2926A=
ENST00000538136.1:c.2673A= (MSH6) ENSP00000438580.1:p.Glu891=
ENST00000540021.5:c.3189A= (MSH6) ENSP00000446475.1:p.Glu1063=
ENST00000614496.4:c.2673A= (MSH6) ENSP00000477844.1:p.Glu891=
ENST00000622629.4:c.483A= (MSH6) ENSP00000482078.1:p.Glu161=
NM_000179.2:c.3579A= , LRG_219t1:c.3579A= (MSH6) NP_000170.1:p.Glu1193=
NM_001281492.1:c.3189A= (MSH6) NP_001268421.1:p.Glu1063=
NM_001281493.1:c.2673A= (MSH6) NP_001268422.1:p.Glu891=
NM_001281494.1:c.2673A= (MSH6) NP_001268423.1:p.Glu891=
XM_005264271.1:c.3282A= (MSH6) XP_005264328.1:p.Glu1094=
XM_011532798.1:c.3396A= (MSH6) XP_011531100.1:p.Glu1132=
XM_011532799.1:c.3282A= (MSH6) XP_011531101.1:p.Glu1094=
XM_011532800.1:c.3282A= (MSH6) XP_011531102.1:p.Glu1094=
XM_024452819.1:c.3579A= (MSH6) XP_024308587.1:p.Glu1193=
XM_024452820.1:c.3396A= (MSH6) XP_024308588.1:p.Glu1132=
XM_024452821.1:c.3282A= (MSH6) XP_024308589.1:p.Glu1094=
XM_024452822.1:c.2673A= (MSH6) XP_024308590.1:p.Glu891=
NM_000179.3:c.3579A= (MSH6) MANE Select NP_000170.1:p.Glu1193=
NM_001281492.2:c.3189A= (MSH6) NP_001268421.1:p.Glu1063=
NM_001281493.2:c.2673A= (MSH6) NP_001268422.1:p.Glu891=
NM_001281494.2:c.2673A= (MSH6) NP_001268423.1:p.Glu891=