Canonical Allele Identifier: CA915942407
Gene: MLH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 666013
dbSNP Id: rs1575376830

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.36993624del , CM000665.2:g.36993624del GRCh38
NC_000003.11:g.37035115del , CM000665.1:g.37035115del GRCh37
NC_000003.10:g.37010119del NCBI36
NG_007109.2:g.5275del , LRG_216:g.5275del
NG_008418.1:g.4681del

Transcript Alleles

HGVS Amino-acid change
ENST00000413740.2:c.77del ENSP00000416476.2:p.Gln26ArgfsTer10
ENST00000450420.6:c.77del ENSP00000393006.2:p.Gln26ArgfsTer10
ENST00000456676.7:c.77del ENSP00000416687.3:p.Gln26ArgfsTer10
ENST00000458009.6:c.77del ENSP00000411066.2:p.Gln26ArgfsTer10
ENST00000616768.6:c.77del ENSP00000480669.3:p.Gln26ArgfsTer10
ENST00000673673.2:c.77del ENSP00000500979.2:p.Gln26ArgfsTer10
ENST00000231790.8:c.77del MANE Select ENSP00000231790.3:p.Gln26ArgfsTer10
ENST00000432299.6:c.77del ENSP00000416783.1:p.Gln26ArgfsTer10
ENST00000442249.6:n.92del
ENST00000673673.1:c.30del
ENST00000673713.1:n.108del
ENST00000673715.1:c.77del ENSP00000501301.1:p.Gln26ArgfsTer10
ENST00000673897.1:c.77del ENSP00000501109.1:p.Gln26ArgfsTer10
ENST00000673899.1:c.77del ENSP00000501030.1:p.Gln26ArgfsTer10
ENST00000673947.1:c.77del ENSP00000501304.1:p.Gln26ArgfsTer10
ENST00000673972.1:c.77del ENSP00000501281.1:p.Gln26ArgfsTer10
ENST00000674111.1:c.77del ENSP00000501162.1:p.Gln26ArgfsTer10
ENST00000231790.6:c.77del ENSP00000231790.2:p.Gln26ArgfsTer10
ENST00000432299.5:c.77del ENSP00000416783.1:p.Gln26ArgfsTer10
ENST00000442249.5:c.77del ENSP00000387511.1:p.Gln26ArgfsTer10
ENST00000454028.5:c.77del ENSP00000392649.1:p.Gln26ArgfsTer10
ENST00000456676.6:c.52del
ENST00000457004.5:c.77del ENSP00000407773.1:p.Gln26ArgfsTer10
ENST00000536378.5:c.-556del ENSP00000444286.2:n.-556del
NM_000249.3:c.77del , LRG_216t1:c.77del NP_000240.1:p.Gln26ArgfsTer10
NM_001258271.1:c.77del NP_001245200.1:p.Gln26ArgfsTer10
NM_001258273.1:c.-556del NP_001245202.1:n.-556del
XM_005265161.1:c.77del XP_005265218.1:p.Gln26ArgfsTer10
XM_005265164.1:c.-642del XP_005265221.1:n.-642del
NM_001167617.2:c.-440del NP_001161089.1:n.-440del
NM_001167618.2:c.-869del NP_001161090.1:n.-869del
NM_001167619.2:c.-782del NP_001161091.1:n.-782del
NM_001258274.2:c.-1019del NP_001245203.1:n.-1019del
NM_001354615.1:c.-550del NP_001341544.1:n.-550del
NM_001354616.1:c.-550del NP_001341545.1:n.-550del
NM_001354617.1:c.-642del NP_001341546.1:n.-642del
NM_001354618.1:c.-874del NP_001341547.1:n.-874del
NM_001354619.1:c.-998del NP_001341548.1:n.-998del
NM_001354620.1:c.-208del NP_001341549.1:n.-208del
NM_001354621.1:c.-967del NP_001341550.1:n.-967del
NM_001354622.1:c.-1080del NP_001341551.1:n.-1080del
NM_001354623.1:c.-989del NP_001341552.1:n.-989del
NM_001354624.1:c.-750del NP_001341553.1:n.-750del
NM_001354625.1:c.-648del NP_001341554.1:n.-648del
NM_001354626.1:c.-745del NP_001341555.1:n.-745del
NM_001354627.1:c.-977del NP_001341556.1:n.-977del
NM_001354628.1:c.77del NP_001341557.1:p.Gln26ArgfsTer10
NM_001354629.1:c.77del NP_001341558.1:p.Gln26ArgfsTer10
NM_001354630.1:c.77del NP_001341559.1:p.Gln26ArgfsTer10
XM_005265161.2:c.77del XP_005265218.1:p.Gln26ArgfsTer10
XM_017006450.2:c.-735del XP_016861939.1:n.-735del
NM_000249.4:c.77del MANE Select NP_000240.1:p.Gln26ArgfsTer10
NM_001167617.3:c.-440del NP_001161089.1:n.-440del
NM_001167618.3:c.-869del NP_001161090.1:n.-869del
NM_001167619.3:c.-782del NP_001161091.1:n.-782del
NM_001258271.2:c.77del NP_001245200.1:p.Gln26ArgfsTer10
NM_001258273.2:c.-556del NP_001245202.1:n.-556del
NM_001258274.3:c.-1019del NP_001245203.1:n.-1019del
NM_001354615.2:c.-550del NP_001341544.1:n.-550del
NM_001354616.2:c.-550del NP_001341545.1:n.-550del
NM_001354617.2:c.-642del NP_001341546.1:n.-642del
NM_001354618.2:c.-874del NP_001341547.1:n.-874del
NM_001354619.2:c.-998del NP_001341548.1:n.-998del
NM_001354620.2:c.-208del NP_001341549.1:n.-208del
NM_001354621.2:c.-967del NP_001341550.1:n.-967del
NM_001354622.2:c.-1080del NP_001341551.1:n.-1080del
NM_001354623.2:c.-989del NP_001341552.1:n.-989del
NM_001354624.2:c.-750del NP_001341553.1:n.-750del
NM_001354625.2:c.-648del NP_001341554.1:n.-648del
NM_001354626.2:c.-745del NP_001341555.1:n.-745del
NM_001354627.2:c.-977del NP_001341556.1:n.-977del
NM_001354628.2:c.77del NP_001341557.1:p.Gln26ArgfsTer10
NM_001354629.2:c.77del NP_001341558.1:p.Gln26ArgfsTer10
NM_001354630.2:c.77del NP_001341559.1:p.Gln26ArgfsTer10