Canonical Allele Identifier: CA352054009
Gene: MLH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1060779
ClinVar RCV Id: RCV001370251
dbSNP Id: rs2125886582

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.37025980A>C , CM000665.2:g.37025980A>C GRCh38
NC_000003.11:g.37067471A>C , CM000665.1:g.37067471A>C GRCh37
NC_000003.10:g.37042475A>C NCBI36
NG_007109.2:g.37631A>C , LRG_216:g.37631A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000413740.2:c.1382A>C ENSP00000416476.2:p.Lys461Thr
ENST00000429117.6:c.1088A>C ENSP00000407019.2:p.Lys363Thr
ENST00000450420.6:c.1382A>C ENSP00000393006.2:p.Lys461Thr
ENST00000456676.7:c.1382A>C ENSP00000416687.3:p.Lys461Thr
ENST00000458009.6:c.*283A>C ENSP00000411066.2:n.*283A>C
ENST00000492474.6:c.659A>C ENSP00000518393.1:p.Lys220Thr
ENST00000616768.6:c.1382A>C ENSP00000480669.3:p.Lys461Thr
ENST00000673673.2:c.1382A>C ENSP00000500979.2:p.Lys461Thr
ENST00000231790.8:c.1382A>C MANE Select ENSP00000231790.3:p.Lys461Thr
ENST00000413212.2:c.*300A>C ENSP00000400844.2:n.*300A>C
ENST00000432299.6:c.*1214A>C ENSP00000416783.1:n.*1214A>C
ENST00000441265.6:c.659A>C ENSP00000398392.2:p.Lys220Thr
ENST00000442249.6:n.1190A>C
ENST00000447829.6:c.*493A>C ENSP00000399329.2:n.*493A>C
ENST00000539477.6:c.659A>C ENSP00000443665.1:p.Lys220Thr
ENST00000616768.5:c.419A>C ENSP00000480669.2:p.Lys140Thr
ENST00000673673.1:c.1335A>C
ENST00000673713.1:n.1506A>C
ENST00000673715.1:c.1382A>C ENSP00000501301.1:p.Lys461Thr
ENST00000673889.1:n.764A>C
ENST00000673897.1:c.*1174A>C ENSP00000501109.1:n.*1174A>C
ENST00000673899.1:c.678-2804A>C ENSP00000501030.1:n.678-2804A>C
ENST00000673947.1:c.*1522A>C ENSP00000501304.1:n.*1522A>C
ENST00000673972.1:c.*1260A>C ENSP00000501281.1:n.*1260A>C
ENST00000673990.1:n.1273A>C
ENST00000674019.1:c.659A>C ENSP00000501081.1:p.Lys220Thr
ENST00000674107.1:n.1230A>C
ENST00000674111.1:c.1382A>C ENSP00000501162.1:p.Lys461Thr
ENST00000231790.6:c.1382A>C ENSP00000231790.2:p.Lys461Thr
ENST00000413212.1:c.457A>C
ENST00000413740.1:c.5A>C ENSP00000416476.1:p.Lys2Thr
ENST00000435176.5:c.1088A>C ENSP00000402564.1:p.Lys363Thr
ENST00000450420.5:c.5A>C ENSP00000393006.1:p.Lys2Thr
ENST00000455445.6:c.659A>C ENSP00000398272.2:p.Lys220Thr
ENST00000456676.6:c.1357A>C
ENST00000458009.5:c.569A>C
ENST00000458205.6:c.659A>C ENSP00000402667.2:p.Lys220Thr
ENST00000536378.5:c.659A>C ENSP00000444286.2:p.Lys220Thr
ENST00000539477.5:c.659A>C ENSP00000443665.1:p.Lys220Thr
ENST00000616768.4:c.150A>C
NM_000249.3:c.1382A>C , LRG_216t1:c.1382A>C NP_000240.1:p.Lys461Thr
NM_001167617.1:c.1088A>C NP_001161089.1:p.Lys363Thr
NM_001167618.1:c.659A>C NP_001161090.1:p.Lys220Thr
NM_001167619.1:c.659A>C NP_001161091.1:p.Lys220Thr
NM_001258271.1:c.1382A>C NP_001245200.1:p.Lys461Thr
NM_001258273.1:c.659A>C NP_001245202.1:p.Lys220Thr
NM_001258274.1:c.659A>C NP_001245203.1:p.Lys220Thr
XM_005265161.1:c.1175A>C XP_005265218.1:p.Lys392Thr
XM_005265163.1:c.659A>C XP_005265220.1:p.Lys220Thr
XM_005265164.1:c.659A>C XP_005265221.1:p.Lys220Thr
XM_005265166.1:c.359A>C XP_005265223.1:p.Lys120Thr
XM_011533727.1:c.308A>C XP_011532029.1:p.Lys103Thr
NM_001167617.2:c.1088A>C NP_001161089.1:p.Lys363Thr
NM_001167618.2:c.659A>C NP_001161090.1:p.Lys220Thr
NM_001167619.2:c.659A>C NP_001161091.1:p.Lys220Thr
NM_001258274.2:c.659A>C NP_001245203.1:p.Lys220Thr
NM_001354615.1:c.659A>C NP_001341544.1:p.Lys220Thr
NM_001354616.1:c.659A>C NP_001341545.1:p.Lys220Thr
NM_001354617.1:c.659A>C NP_001341546.1:p.Lys220Thr
NM_001354618.1:c.659A>C NP_001341547.1:p.Lys220Thr
NM_001354619.1:c.659A>C NP_001341548.1:p.Lys220Thr
NM_001354620.1:c.1088A>C NP_001341549.1:p.Lys363Thr
NM_001354621.1:c.359A>C NP_001341550.1:p.Lys120Thr
NM_001354622.1:c.359A>C NP_001341551.1:p.Lys120Thr
NM_001354623.1:c.359A>C NP_001341552.1:p.Lys120Thr
NM_001354624.1:c.308A>C NP_001341553.1:p.Lys103Thr
NM_001354625.1:c.308A>C NP_001341554.1:p.Lys103Thr
NM_001354626.1:c.308A>C NP_001341555.1:p.Lys103Thr
NM_001354627.1:c.308A>C NP_001341556.1:p.Lys103Thr
NM_001354628.1:c.1382A>C NP_001341557.1:p.Lys461Thr
NM_001354629.1:c.1283A>C NP_001341558.1:p.Lys428Thr
NM_001354630.1:c.1382A>C NP_001341559.1:p.Lys461Thr
XM_005265161.2:c.1175A>C XP_005265218.1:p.Lys392Thr
XM_017006450.2:c.359A>C XP_016861939.1:p.Lys120Thr
NM_000249.4:c.1382A>C MANE Select NP_000240.1:p.Lys461Thr
NM_001167617.3:c.1088A>C NP_001161089.1:p.Lys363Thr
NM_001167618.3:c.659A>C NP_001161090.1:p.Lys220Thr
NM_001167619.3:c.659A>C NP_001161091.1:p.Lys220Thr
NM_001258271.2:c.1382A>C NP_001245200.1:p.Lys461Thr
NM_001258273.2:c.659A>C NP_001245202.1:p.Lys220Thr
NM_001258274.3:c.659A>C NP_001245203.1:p.Lys220Thr
NM_001354615.2:c.659A>C NP_001341544.1:p.Lys220Thr
NM_001354616.2:c.659A>C NP_001341545.1:p.Lys220Thr
NM_001354617.2:c.659A>C NP_001341546.1:p.Lys220Thr
NM_001354618.2:c.659A>C NP_001341547.1:p.Lys220Thr
NM_001354619.2:c.659A>C NP_001341548.1:p.Lys220Thr
NM_001354620.2:c.1088A>C NP_001341549.1:p.Lys363Thr
NM_001354621.2:c.359A>C NP_001341550.1:p.Lys120Thr
NM_001354622.2:c.359A>C NP_001341551.1:p.Lys120Thr
NM_001354623.2:c.359A>C NP_001341552.1:p.Lys120Thr
NM_001354624.2:c.308A>C NP_001341553.1:p.Lys103Thr
NM_001354625.2:c.308A>C NP_001341554.1:p.Lys103Thr
NM_001354626.2:c.308A>C NP_001341555.1:p.Lys103Thr
NM_001354627.2:c.308A>C NP_001341556.1:p.Lys103Thr
NM_001354628.2:c.1382A>C NP_001341557.1:p.Lys461Thr
NM_001354629.2:c.1283A>C NP_001341558.1:p.Lys428Thr
NM_001354630.2:c.1382A>C NP_001341559.1:p.Lys461Thr