Canonical Allele Identifier: CA010983

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47800815_47800816del , CM000664.2:g.47800815_47800816del GRCh38
NC_000002.11:g.48027954_48027955del , CM000664.1:g.48027954_48027955del GRCh37
NC_000002.10:g.47881458_47881459del NCBI36
NG_007111.1:g.22669_22670del , LRG_219:g.22669_22670del

Transcript Alleles

HGVS Amino-acid Change
NM_000179.3:c.2832_2833del (MSH6) MANE Select NP_000170.1:p.Ile944MetfsTer4
ENST00000234420.11:c.2832_2833del (MSH6) MANE Select ENSP00000234420.5:p.Ile944MetfsTer4
NM_000179.2:c.2832_2833del , LRG_219t1:c.2832_2833del (MSH6) NP_000170.1:p.Ile944MetfsTer4
NM_001281492.1:c.2442_2443del (MSH6) NP_001268421.1:p.Ile814MetfsTer4
NM_001281492.2:c.2442_2443del (MSH6) NP_001268421.1:p.Ile814MetfsTer4
NM_001281493.1:c.1926_1927del (MSH6) NP_001268422.1:p.Ile642MetfsTer4
NM_001281493.2:c.1926_1927del (MSH6) NP_001268422.1:p.Ile642MetfsTer4
NM_001281494.1:c.1926_1927del (MSH6) NP_001268423.1:p.Ile642MetfsTer4
NM_001281494.2:c.1926_1927del (MSH6) NP_001268423.1:p.Ile642MetfsTer4
ENST00000234420.9:c.2832_2833del (MSH6) ENSP00000234420.4:p.Ile944MetfsTer4
ENST00000405808.5:c.169+7379_169+7380del (FBXO11) ENSP00000385127.1:n.169+7379_169+7380del
ENST00000411819.2:c.2535_2536del (MSH6) ENSP00000406248.2:p.Ile845MetfsTer4
ENST00000420813.6:c.2535_2536del (MSH6) ENSP00000390382.2:p.Ile845MetfsTer4
ENST00000434234.5:c.*124+7178_*124+7179del (FBXO11) ENSP00000402692.1:n.*124+7178_*124+7179del
ENST00000445503.5:c.*2179_*2180del (MSH6) ENSP00000405294.1:n.*2179_*2180del
ENST00000455383.6:c.2535_2536del (MSH6) ENSP00000397484.2:p.Ile845MetfsTer4
ENST00000538136.1:c.1926_1927del (MSH6) ENSP00000438580.1:p.Ile642MetfsTer4
ENST00000540021.5:c.2442_2443del (MSH6) ENSP00000446475.1:p.Ile814MetfsTer4
ENST00000540021.6:c.2442_2443del (MSH6) ENSP00000446475.1:p.Ile814MetfsTer4
ENST00000614496.4:c.1926_1927del (MSH6) ENSP00000477844.1:p.Ile642MetfsTer4
ENST00000616033.4:c.2829_2830del (MSH6) ENSP00000480261.1:p.Ile943MetfsTer4
ENST00000622629.4:c.-265_-264del (MSH6) ENSP00000482078.1:n.-265_-264del
ENST00000652107.1:c.2535_2536del (MSH6) ENSP00000498629.1:p.Ile845MetfsTer4
ENST00000673637.1:c.2535_2536del (MSH6) ENSP00000501310.1:p.Ile845MetfsTer4
ENST00000699999.1:n.2916_2917del (MSH6)
ENST00000700000.1:c.1606+1226_1606+1227del (MSH6) ENSP00000514749.1:n.1606+1226_1606+1227del
ENST00000700002.1:c.2838_2839del (MSH6) ENSP00000514750.1:p.Ile946MetfsTer4
ENST00000700003.1:c.628-2605_628-2604del (MSH6) ENSP00000514751.1:n.628-2605_628-2604del
ENST00000700004.1:c.1989_1990del (MSH6) ENSP00000514752.1:p.Ile663MetfsTer4
ENST00000700004.2:c.2832_2833del (MSH6) ENSP00000514752.2:p.Ile944MetfsTer4
XM_005264271.1:c.2535_2536del (MSH6) XP_005264328.1:p.Ile845MetfsTer4
XM_011532798.1:c.2649_2650del (MSH6) XP_011531100.1:p.Ile883MetfsTer4
XM_011532799.1:c.2535_2536del (MSH6) XP_011531101.1:p.Ile845MetfsTer4
XM_011532800.1:c.2535_2536del (MSH6) XP_011531102.1:p.Ile845MetfsTer4
XM_024452819.1:c.2832_2833del (MSH6) XP_024308587.1:p.Ile944MetfsTer4
XM_024452820.1:c.2649_2650del (MSH6) XP_024308588.1:p.Ile883MetfsTer4
XM_024452821.1:c.2535_2536del (MSH6) XP_024308589.1:p.Ile845MetfsTer4
XM_024452822.1:c.1926_1927del (MSH6) XP_024308590.1:p.Ile642MetfsTer4