Canonical Allele Identifier: CA2838233007

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47798775dup , CM000664.2:g.47798775dup GRCh38
NC_000002.11:g.48025914dup , CM000664.1:g.48025914dup GRCh37
NC_000002.10:g.47879418dup NCBI36
NG_007111.1:g.20629dup , LRG_219:g.20629dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.495dup (MSH6) ENSP00000406248.2:p.Phe166IlefsTer2
ENST00000420813.6:c.495dup (MSH6) ENSP00000390382.2:p.Phe166IlefsTer2
ENST00000455383.6:c.495dup (MSH6) ENSP00000397484.2:p.Phe166IlefsTer2
ENST00000700004.2:c.792dup (MSH6) ENSP00000514752.2:p.Phe265IlefsTer2
ENST00000699999.1:n.876dup (MSH6)
ENST00000700000.1:c.792dup (MSH6) ENSP00000514749.1:p.Phe265IlefsTer2
ENST00000700002.1:c.798dup (MSH6) ENSP00000514750.1:p.Phe267IlefsTer2
ENST00000700003.1:c.627+2712dup (MSH6) ENSP00000514751.1:n.627+2712dup
ENST00000234420.11:c.792dup (MSH6) MANE Select ENSP00000234420.5:p.Phe265IlefsTer2
ENST00000540021.6:c.402dup (MSH6) ENSP00000446475.1:p.Phe135IlefsTer2
ENST00000652107.1:c.495dup (MSH6) ENSP00000498629.1:p.Phe166IlefsTer2
ENST00000673637.1:c.495dup (MSH6) ENSP00000501310.1:p.Phe166IlefsTer2
ENST00000673922.1:n.514dup (MSH6)
ENST00000234420.9:c.792dup (MSH6) ENSP00000234420.4:p.Phe265IlefsTer2
ENST00000405808.5:c.170-9334dup (FBXO11) ENSP00000385127.1:n.170-9334dup
ENST00000434234.5:c.*124+9220dup (FBXO11) ENSP00000402692.1:n.*124+9220dup
ENST00000445503.5:c.*139dup (MSH6) ENSP00000405294.1:n.*139dup
ENST00000456246.1:c.*280dup (MSH6) ENSP00000410570.1:n.*280dup
ENST00000538136.1:c.-115dup (MSH6) ENSP00000438580.1:n.-115dup
ENST00000540021.5:c.402dup (MSH6) ENSP00000446475.1:p.Phe135IlefsTer2
ENST00000614496.4:c.-115dup (MSH6) ENSP00000477844.1:n.-115dup
ENST00000616033.4:c.789dup (MSH6) ENSP00000480261.1:p.Phe264IlefsTer2
ENST00000622629.4:c.-2305dup (MSH6) ENSP00000482078.1:n.-2305dup
NM_000179.2:c.792dup , LRG_219t1:c.792dup (MSH6) NP_000170.1:p.Phe265IlefsTer2
NM_001281492.1:c.402dup (MSH6) NP_001268421.1:p.Phe135IlefsTer2
NM_001281493.1:c.-115dup (MSH6) NP_001268422.1:n.-115dup
NM_001281494.1:c.-115dup (MSH6) NP_001268423.1:n.-115dup
XM_005264271.1:c.495dup (MSH6) XP_005264328.1:p.Phe166IlefsTer2
XM_011532798.1:c.609dup (MSH6) XP_011531100.1:p.Phe204IlefsTer2
XM_011532799.1:c.495dup (MSH6) XP_011531101.1:p.Phe166IlefsTer2
XM_011532800.1:c.495dup (MSH6) XP_011531102.1:p.Phe166IlefsTer2
XM_024452819.1:c.792dup (MSH6) XP_024308587.1:p.Phe265IlefsTer2
XM_024452820.1:c.609dup (MSH6) XP_024308588.1:p.Phe204IlefsTer2
XM_024452821.1:c.495dup (MSH6) XP_024308589.1:p.Phe166IlefsTer2
XM_024452822.1:c.-115dup (MSH6) XP_024308590.1:n.-115dup
NM_000179.3:c.792dup (MSH6) MANE Select NP_000170.1:p.Phe265IlefsTer2
NM_001281492.2:c.402dup (MSH6) NP_001268421.1:p.Phe135IlefsTer2
NM_001281493.2:c.-115dup (MSH6) NP_001268422.1:n.-115dup
NM_001281494.2:c.-115dup (MSH6) NP_001268423.1:n.-115dup