Canonical Allele Identifier: CA2496053496

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47805658C= , CM000664.2:g.47805658C= GRCh38
NC_000002.11:g.48032797C= , CM000664.1:g.48032797C= GRCh37
NC_000002.10:g.47886301C= NCBI36
NG_007111.1:g.27512C= , LRG_219:g.27512C=
NG_008397.1:g.105018G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.3300C= (MSH6) ENSP00000406248.2:p.Ser1100=
ENST00000420813.6:c.3300C= (MSH6) ENSP00000390382.2:p.Ser1100=
ENST00000455383.6:c.3300C= (MSH6) ENSP00000397484.2:p.Ser1100=
ENST00000700004.2:c.3213C= (MSH6) ENSP00000514752.2:p.Ser1071=
ENST00000699999.1:n.4271C= (MSH6)
ENST00000700000.1:c.2031C= (MSH6) ENSP00000514749.1:p.Ser677=
ENST00000700002.1:c.3603C= (MSH6) ENSP00000514750.1:p.Ser1201=
ENST00000700003.1:c.1052C= (MSH6) ENSP00000514751.1:n.1052C=
ENST00000700004.1:c.2370C= (MSH6) ENSP00000514752.1:p.Ser790=
ENST00000700005.1:n.2448C= (MSH6)
ENST00000700006.1:n.4259C= (MSH6)
ENST00000700007.1:n.2192C= (MSH6)
ENST00000700008.1:n.1766C= (MSH6)
ENST00000700009.1:n.1765C= (MSH6)
ENST00000700010.1:n.1006C= (MSH6)
ENST00000700011.1:n.2891C= (MSH6)
ENST00000234420.11:c.3597C= (MSH6) MANE Select ENSP00000234420.5:p.Ser1199=
ENST00000540021.6:c.3207C= (MSH6) ENSP00000446475.1:p.Ser1069=
ENST00000652107.1:c.3300C= (MSH6) ENSP00000498629.1:p.Ser1100=
ENST00000673637.1:c.3300C= (MSH6) ENSP00000501310.1:p.Ser1100=
ENST00000234420.9:c.3597C= (MSH6) ENSP00000234420.4:p.Ser1199=
ENST00000405808.5:c.169+2537G= (FBXO11) ENSP00000385127.1:n.169+2537G=
ENST00000434234.5:c.*124+2336G= (FBXO11) ENSP00000402692.1:n.*124+2336G=
ENST00000445503.5:c.*2944C= (MSH6) ENSP00000405294.1:n.*2944C=
ENST00000538136.1:c.2691C= (MSH6) ENSP00000438580.1:p.Ser897=
ENST00000540021.5:c.3207C= (MSH6) ENSP00000446475.1:p.Ser1069=
ENST00000614496.4:c.2691C= (MSH6) ENSP00000477844.1:p.Ser897=
ENST00000622629.4:c.501C= (MSH6) ENSP00000482078.1:p.Ser167=
NM_000179.2:c.3597C= , LRG_219t1:c.3597C= (MSH6) NP_000170.1:p.Ser1199=
NM_001281492.1:c.3207C= (MSH6) NP_001268421.1:p.Ser1069=
NM_001281493.1:c.2691C= (MSH6) NP_001268422.1:p.Ser897=
NM_001281494.1:c.2691C= (MSH6) NP_001268423.1:p.Ser897=
XM_005264271.1:c.3300C= (MSH6) XP_005264328.1:p.Ser1100=
XM_011532798.1:c.3414C= (MSH6) XP_011531100.1:p.Ser1138=
XM_011532799.1:c.3300C= (MSH6) XP_011531101.1:p.Ser1100=
XM_011532800.1:c.3300C= (MSH6) XP_011531102.1:p.Ser1100=
XM_024452819.1:c.3597C= (MSH6) XP_024308587.1:p.Ser1199=
XM_024452820.1:c.3414C= (MSH6) XP_024308588.1:p.Ser1138=
XM_024452821.1:c.3300C= (MSH6) XP_024308589.1:p.Ser1100=
XM_024452822.1:c.2691C= (MSH6) XP_024308590.1:p.Ser897=
NM_000179.3:c.3597C= (MSH6) MANE Select NP_000170.1:p.Ser1199=
NM_001281492.2:c.3207C= (MSH6) NP_001268421.1:p.Ser1069=
NM_001281493.2:c.2691C= (MSH6) NP_001268422.1:p.Ser897=
NM_001281494.2:c.2691C= (MSH6) NP_001268423.1:p.Ser897=