Canonical Allele Identifier: CA1357864771
Gene: MLH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.36993528T= , CM000665.2:g.36993528T= GRCh38
NC_000003.11:g.37035019T= , CM000665.1:g.37035019T= GRCh37
NC_000003.10:g.37010023T= NCBI36
NG_007109.2:g.5179T= , LRG_216:g.5179T=
NG_008418.1:g.4777A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000413740.2:c.-20T= ENSP00000416476.2:n.-20T=
ENST00000450420.6:c.-20T= ENSP00000393006.2:n.-20T=
ENST00000456676.7:c.-20T= ENSP00000416687.3:n.-20T=
ENST00000458009.6:c.-20T= ENSP00000411066.2:n.-20T=
ENST00000616768.6:c.-20T= ENSP00000480669.3:n.-20T=
ENST00000673673.2:c.-20T= ENSP00000500979.2:n.-20T=
ENST00000231790.8:c.-20T= MANE Select ENSP00000231790.3:n.-20T=
ENST00000432299.6:c.-20T= ENSP00000416783.1:n.-20T=
ENST00000673713.1:n.12T=
ENST00000673715.1:c.-20T= ENSP00000501301.1:n.-20T=
ENST00000673899.1:c.-20T= ENSP00000501030.1:n.-20T=
ENST00000673972.1:c.-20T= ENSP00000501281.1:n.-20T=
ENST00000674111.1:c.-20T= ENSP00000501162.1:n.-20T=
ENST00000231790.6:c.-20T= ENSP00000231790.2:n.-20T=
ENST00000432299.5:c.-20T= ENSP00000416783.1:n.-20T=
ENST00000457004.5:c.-20T= ENSP00000407773.1:n.-20T=
ENST00000536378.5:c.-652T= ENSP00000444286.2:n.-652T=
NM_000249.3:c.-20T= , LRG_216t1:c.-20T= NP_000240.1:n.-20T=
NM_001258271.1:c.-20T= NP_001245200.1:n.-20T=
NM_001258273.1:c.-652T= NP_001245202.1:n.-652T=
XM_005265161.1:c.-20T= XP_005265218.1:n.-20T=
XM_005265164.1:c.-738T= XP_005265221.1:n.-738T=
NM_001167617.2:c.-536T= NP_001161089.1:n.-536T=
NM_001167618.2:c.-965T= NP_001161090.1:n.-965T=
NM_001167619.2:c.-878T= NP_001161091.1:n.-878T=
NM_001258274.2:c.-1115T= NP_001245203.1:n.-1115T=
NM_001354615.1:c.-646T= NP_001341544.1:n.-646T=
NM_001354616.1:c.-646T= NP_001341545.1:n.-646T=
NM_001354617.1:c.-738T= NP_001341546.1:n.-738T=
NM_001354618.1:c.-970T= NP_001341547.1:n.-970T=
NM_001354619.1:c.-1094T= NP_001341548.1:n.-1094T=
NM_001354620.1:c.-304T= NP_001341549.1:n.-304T=
NM_001354621.1:c.-1063T= NP_001341550.1:n.-1063T=
NM_001354622.1:c.-1176T= NP_001341551.1:n.-1176T=
NM_001354623.1:c.-1085T= NP_001341552.1:n.-1085T=
NM_001354624.1:c.-846T= NP_001341553.1:n.-846T=
NM_001354625.1:c.-744T= NP_001341554.1:n.-744T=
NM_001354626.1:c.-841T= NP_001341555.1:n.-841T=
NM_001354627.1:c.-1073T= NP_001341556.1:n.-1073T=
NM_001354628.1:c.-20T= NP_001341557.1:n.-20T=
NM_001354629.1:c.-20T= NP_001341558.1:n.-20T=
NM_001354630.1:c.-20T= NP_001341559.1:n.-20T=
XM_005265161.2:c.-20T= XP_005265218.1:n.-20T=
XM_017006450.2:c.-831T= XP_016861939.1:n.-831T=
NM_000249.4:c.-20T= MANE Select NP_000240.1:n.-20T=
NM_001167617.3:c.-536T= NP_001161089.1:n.-536T=
NM_001167618.3:c.-965T= NP_001161090.1:n.-965T=
NM_001167619.3:c.-878T= NP_001161091.1:n.-878T=
NM_001258271.2:c.-20T= NP_001245200.1:n.-20T=
NM_001258273.2:c.-652T= NP_001245202.1:n.-652T=
NM_001258274.3:c.-1115T= NP_001245203.1:n.-1115T=
NM_001354615.2:c.-646T= NP_001341544.1:n.-646T=
NM_001354616.2:c.-646T= NP_001341545.1:n.-646T=
NM_001354617.2:c.-738T= NP_001341546.1:n.-738T=
NM_001354618.2:c.-970T= NP_001341547.1:n.-970T=
NM_001354619.2:c.-1094T= NP_001341548.1:n.-1094T=
NM_001354620.2:c.-304T= NP_001341549.1:n.-304T=
NM_001354621.2:c.-1063T= NP_001341550.1:n.-1063T=
NM_001354622.2:c.-1176T= NP_001341551.1:n.-1176T=
NM_001354623.2:c.-1085T= NP_001341552.1:n.-1085T=
NM_001354624.2:c.-846T= NP_001341553.1:n.-846T=
NM_001354625.2:c.-744T= NP_001341554.1:n.-744T=
NM_001354626.2:c.-841T= NP_001341555.1:n.-841T=
NM_001354627.2:c.-1073T= NP_001341556.1:n.-1073T=
NM_001354628.2:c.-20T= NP_001341557.1:n.-20T=
NM_001354629.2:c.-20T= NP_001341558.1:n.-20T=
NM_001354630.2:c.-20T= NP_001341559.1:n.-20T=