Canonical Allele Identifier: CA1357864854
Gene: MLH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.36993610G= , CM000665.2:g.36993610G= GRCh38
NC_000003.11:g.37035101G= , CM000665.1:g.37035101G= GRCh37
NC_000003.10:g.37010105G= NCBI36
NG_007109.2:g.5261G= , LRG_216:g.5261G=
NG_008418.1:g.4695C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000413740.2:c.63G= ENSP00000416476.2:p.Ala21=
ENST00000450420.6:c.63G= ENSP00000393006.2:p.Ala21=
ENST00000456676.7:c.63G= ENSP00000416687.3:p.Ala21=
ENST00000458009.6:c.63G= ENSP00000411066.2:p.Ala21=
ENST00000616768.6:c.63G= ENSP00000480669.3:p.Ala21=
ENST00000673673.2:c.63G= ENSP00000500979.2:p.Ala21=
ENST00000231790.8:c.63G= MANE Select ENSP00000231790.3:p.Ala21=
ENST00000432299.6:c.63G= ENSP00000416783.1:p.Ala21=
ENST00000442249.6:n.78G=
ENST00000673673.1:c.16G=
ENST00000673713.1:n.94G=
ENST00000673715.1:c.63G= ENSP00000501301.1:p.Ala21=
ENST00000673897.1:c.63G= ENSP00000501109.1:p.Ala21=
ENST00000673899.1:c.63G= ENSP00000501030.1:p.Ala21=
ENST00000673947.1:c.63G= ENSP00000501304.1:p.Ala21=
ENST00000673972.1:c.63G= ENSP00000501281.1:p.Ala21=
ENST00000674111.1:c.63G= ENSP00000501162.1:p.Ala21=
ENST00000231790.6:c.63G= ENSP00000231790.2:p.Ala21=
ENST00000432299.5:c.63G= ENSP00000416783.1:p.Ala21=
ENST00000442249.5:c.63G= ENSP00000387511.1:p.Ala21=
ENST00000454028.5:c.63G= ENSP00000392649.1:p.Ala21=
ENST00000456676.6:c.38G=
ENST00000457004.5:c.63G= ENSP00000407773.1:p.Ala21=
ENST00000536378.5:c.-570G= ENSP00000444286.2:n.-570G=
NM_000249.3:c.63G= , LRG_216t1:c.63G= NP_000240.1:p.Ala21=
NM_001258271.1:c.63G= NP_001245200.1:p.Ala21=
NM_001258273.1:c.-570G= NP_001245202.1:n.-570G=
XM_005265161.1:c.63G= XP_005265218.1:p.Ala21=
XM_005265164.1:c.-656G= XP_005265221.1:n.-656G=
NM_001167617.2:c.-454G= NP_001161089.1:n.-454G=
NM_001167618.2:c.-883G= NP_001161090.1:n.-883G=
NM_001167619.2:c.-796G= NP_001161091.1:n.-796G=
NM_001258274.2:c.-1033G= NP_001245203.1:n.-1033G=
NM_001354615.1:c.-564G= NP_001341544.1:n.-564G=
NM_001354616.1:c.-564G= NP_001341545.1:n.-564G=
NM_001354617.1:c.-656G= NP_001341546.1:n.-656G=
NM_001354618.1:c.-888G= NP_001341547.1:n.-888G=
NM_001354619.1:c.-1012G= NP_001341548.1:n.-1012G=
NM_001354620.1:c.-222G= NP_001341549.1:n.-222G=
NM_001354621.1:c.-981G= NP_001341550.1:n.-981G=
NM_001354622.1:c.-1094G= NP_001341551.1:n.-1094G=
NM_001354623.1:c.-1003G= NP_001341552.1:n.-1003G=
NM_001354624.1:c.-764G= NP_001341553.1:n.-764G=
NM_001354625.1:c.-662G= NP_001341554.1:n.-662G=
NM_001354626.1:c.-759G= NP_001341555.1:n.-759G=
NM_001354627.1:c.-991G= NP_001341556.1:n.-991G=
NM_001354628.1:c.63G= NP_001341557.1:p.Ala21=
NM_001354629.1:c.63G= NP_001341558.1:p.Ala21=
NM_001354630.1:c.63G= NP_001341559.1:p.Ala21=
XM_005265161.2:c.63G= XP_005265218.1:p.Ala21=
XM_017006450.2:c.-749G= XP_016861939.1:n.-749G=
NM_000249.4:c.63G= MANE Select NP_000240.1:p.Ala21=
NM_001167617.3:c.-454G= NP_001161089.1:n.-454G=
NM_001167618.3:c.-883G= NP_001161090.1:n.-883G=
NM_001167619.3:c.-796G= NP_001161091.1:n.-796G=
NM_001258271.2:c.63G= NP_001245200.1:p.Ala21=
NM_001258273.2:c.-570G= NP_001245202.1:n.-570G=
NM_001258274.3:c.-1033G= NP_001245203.1:n.-1033G=
NM_001354615.2:c.-564G= NP_001341544.1:n.-564G=
NM_001354616.2:c.-564G= NP_001341545.1:n.-564G=
NM_001354617.2:c.-656G= NP_001341546.1:n.-656G=
NM_001354618.2:c.-888G= NP_001341547.1:n.-888G=
NM_001354619.2:c.-1012G= NP_001341548.1:n.-1012G=
NM_001354620.2:c.-222G= NP_001341549.1:n.-222G=
NM_001354621.2:c.-981G= NP_001341550.1:n.-981G=
NM_001354622.2:c.-1094G= NP_001341551.1:n.-1094G=
NM_001354623.2:c.-1003G= NP_001341552.1:n.-1003G=
NM_001354624.2:c.-764G= NP_001341553.1:n.-764G=
NM_001354625.2:c.-662G= NP_001341554.1:n.-662G=
NM_001354626.2:c.-759G= NP_001341555.1:n.-759G=
NM_001354627.2:c.-991G= NP_001341556.1:n.-991G=
NM_001354628.2:c.63G= NP_001341557.1:p.Ala21=
NM_001354629.2:c.63G= NP_001341558.1:p.Ala21=
NM_001354630.2:c.63G= NP_001341559.1:p.Ala21=