Canonical Allele Identifier: CA2499216711
Gene: MLH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1076321
dbSNP Id: rs2125986083

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.37047675del , CM000665.2:g.37047675del GRCh38
NC_000003.11:g.37089166del , CM000665.1:g.37089166del GRCh37
NC_000003.10:g.37064170del NCBI36
NG_007109.2:g.59326del , LRG_216:g.59326del

Transcript Alleles

HGVS Amino-acid Change
ENST00000413740.2:c.1668-2811del ENSP00000416476.2:n.1668-2811del
ENST00000429117.6:c.1594del ENSP00000407019.2:p.Ile532LeufsTer7
ENST00000450420.6:c.1559-2811del ENSP00000393006.2:n.1559-2811del
ENST00000456676.7:c.1888del ENSP00000416687.3:p.Ile630LeufsTer?
ENST00000492474.6:c.1165del ENSP00000518393.1:p.Ile389LeufsTer7
ENST00000616768.6:c.1888del ENSP00000480669.3:p.Ile630LeufsTer4
ENST00000673673.2:c.1732-842del ENSP00000500979.2:n.1732-842del
ENST00000231790.8:c.1888del MANE Select ENSP00000231790.3:p.Ile630LeufsTer7
ENST00000413212.2:c.*806del ENSP00000400844.2:n.*806del
ENST00000432299.6:c.*1720del ENSP00000416783.1:n.*1720del
ENST00000441265.6:c.*117del ENSP00000398392.2:n.*117del
ENST00000447829.6:c.*999del ENSP00000399329.2:n.*999del
ENST00000539477.6:c.1165del ENSP00000443665.1:p.Ile389LeufsTer7
ENST00000616768.5:c.925del ENSP00000480669.2:p.Ile309LeufsTer4
ENST00000673673.1:c.1685-842del
ENST00000673715.1:c.1888del ENSP00000501301.1:p.Ile630LeufsTer17
ENST00000673741.1:n.922del
ENST00000673889.1:n.1270del
ENST00000673897.1:c.*1680del ENSP00000501109.1:n.*1680del
ENST00000673899.1:c.1156del ENSP00000501030.1:p.Ile386LeufsTer7
ENST00000673947.1:c.*2028del ENSP00000501304.1:n.*2028del
ENST00000673972.1:c.*1766del ENSP00000501281.1:n.*1766del
ENST00000674019.1:c.1165del ENSP00000501081.1:p.Ile389LeufsTer7
ENST00000674111.1:c.*117del ENSP00000501162.1:n.*117del
ENST00000674125.1:n.599del
ENST00000231790.6:c.1888del ENSP00000231790.2:p.Ile630LeufsTer7
ENST00000413740.1:c.291-2811del ENSP00000416476.1:n.291-2811del
ENST00000435176.5:c.1594del ENSP00000402564.1:p.Ile532LeufsTer7
ENST00000450420.5:c.182-2811del ENSP00000393006.1:n.182-2811del
ENST00000455445.6:c.1165del ENSP00000398272.2:p.Ile389LeufsTer7
ENST00000456676.6:c.1863del
ENST00000458205.6:c.1165del ENSP00000402667.2:p.Ile389LeufsTer7
ENST00000536378.5:c.1165del ENSP00000444286.2:p.Ile389LeufsTer7
ENST00000539477.5:c.1165del ENSP00000443665.1:p.Ile389LeufsTer7
ENST00000616768.4:c.656del
NM_000249.3:c.1888del , LRG_216t1:c.1888del NP_000240.1:p.Ile630LeufsTer7
NM_001167617.1:c.1594del NP_001161089.1:p.Ile532LeufsTer7
NM_001167618.1:c.1165del NP_001161090.1:p.Ile389LeufsTer7
NM_001167619.1:c.1165del NP_001161091.1:p.Ile389LeufsTer7
NM_001258271.1:c.1888del NP_001245200.1:p.Ile630LeufsTer?
NM_001258273.1:c.1165del NP_001245202.1:p.Ile389LeufsTer7
NM_001258274.1:c.1165del NP_001245203.1:p.Ile389LeufsTer7
XM_005265161.1:c.1681del XP_005265218.1:p.Ile561LeufsTer7
XM_005265163.1:c.1165del XP_005265220.1:p.Ile389LeufsTer7
XM_005265164.1:c.1165del XP_005265221.1:p.Ile389LeufsTer7
XM_005265166.1:c.865del XP_005265223.1:p.Ile289LeufsTer7
XM_011533727.1:c.814del XP_011532029.1:p.Ile272LeufsTer7
NM_001167617.2:c.1594del NP_001161089.1:p.Ile532LeufsTer7
NM_001167618.2:c.1165del NP_001161090.1:p.Ile389LeufsTer7
NM_001167619.2:c.1165del NP_001161091.1:p.Ile389LeufsTer7
NM_001258274.2:c.1165del NP_001245203.1:p.Ile389LeufsTer7
NM_001354615.1:c.1165del NP_001341544.1:p.Ile389LeufsTer7
NM_001354616.1:c.1165del NP_001341545.1:p.Ile389LeufsTer7
NM_001354617.1:c.1165del NP_001341546.1:p.Ile389LeufsTer7
NM_001354618.1:c.1165del NP_001341547.1:p.Ile389LeufsTer7
NM_001354619.1:c.1165del NP_001341548.1:p.Ile389LeufsTer7
NM_001354620.1:c.1594del NP_001341549.1:p.Ile532LeufsTer7
NM_001354621.1:c.865del NP_001341550.1:p.Ile289LeufsTer7
NM_001354622.1:c.865del NP_001341551.1:p.Ile289LeufsTer7
NM_001354623.1:c.865del NP_001341552.1:p.Ile289LeufsTer7
NM_001354624.1:c.814del NP_001341553.1:p.Ile272LeufsTer7
NM_001354625.1:c.814del NP_001341554.1:p.Ile272LeufsTer7
NM_001354626.1:c.814del NP_001341555.1:p.Ile272LeufsTer7
NM_001354627.1:c.814del NP_001341556.1:p.Ile272LeufsTer7
NM_001354628.1:c.1888del NP_001341557.1:p.Ile630LeufsTer4
NM_001354629.1:c.1789del NP_001341558.1:p.Ile597LeufsTer7
NM_001354630.1:c.1732-842del NP_001341559.1:n.1732-842del
XM_005265161.2:c.1681del XP_005265218.1:p.Ile561LeufsTer7
XM_017006450.2:c.865del XP_016861939.1:p.Ile289LeufsTer7
NM_000249.4:c.1888del MANE Select NP_000240.1:p.Ile630LeufsTer7
NM_001167617.3:c.1594del NP_001161089.1:p.Ile532LeufsTer7
NM_001167618.3:c.1165del NP_001161090.1:p.Ile389LeufsTer7
NM_001167619.3:c.1165del NP_001161091.1:p.Ile389LeufsTer7
NM_001258271.2:c.1888del NP_001245200.1:p.Ile630LeufsTer?
NM_001258273.2:c.1165del NP_001245202.1:p.Ile389LeufsTer7
NM_001258274.3:c.1165del NP_001245203.1:p.Ile389LeufsTer7
NM_001354615.2:c.1165del NP_001341544.1:p.Ile389LeufsTer7
NM_001354616.2:c.1165del NP_001341545.1:p.Ile389LeufsTer7
NM_001354617.2:c.1165del NP_001341546.1:p.Ile389LeufsTer7
NM_001354618.2:c.1165del NP_001341547.1:p.Ile389LeufsTer7
NM_001354619.2:c.1165del NP_001341548.1:p.Ile389LeufsTer7
NM_001354620.2:c.1594del NP_001341549.1:p.Ile532LeufsTer7
NM_001354621.2:c.865del NP_001341550.1:p.Ile289LeufsTer7
NM_001354622.2:c.865del NP_001341551.1:p.Ile289LeufsTer7
NM_001354623.2:c.865del NP_001341552.1:p.Ile289LeufsTer7
NM_001354624.2:c.814del NP_001341553.1:p.Ile272LeufsTer7
NM_001354625.2:c.814del NP_001341554.1:p.Ile272LeufsTer7
NM_001354626.2:c.814del NP_001341555.1:p.Ile272LeufsTer7
NM_001354627.2:c.814del NP_001341556.1:p.Ile272LeufsTer7
NM_001354628.2:c.1888del NP_001341557.1:p.Ile630LeufsTer4
NM_001354629.2:c.1789del NP_001341558.1:p.Ile597LeufsTer7
NM_001354630.2:c.1732-842del NP_001341559.1:n.1732-842del