Canonical Allele Identifier: CA352052725

Gene: MLH1

Linked Data

• dbSNP Id: rs2083425872
• MyVariant Identifiers: chr3:g.37067329G>C (hg19) ; chr3:g.37025838G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.37025838G>C , CM000665.2:g.37025838G>C	GRCh38
NC_000003.11:g.37067329G>C , CM000665.1:g.37067329G>C	GRCh37
NC_000003.10:g.37042333G>C	NCBI36
NG_007109.2:g.37489G>C , LRG_216:g.37489G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413740.2:c.1240G>C	ENSP00000416476.2:p.Glu414Gln
ENST00000429117.6:c.946G>C	ENSP00000407019.2:p.Glu316Gln
ENST00000450420.6:c.1240G>C	ENSP00000393006.2:p.Glu414Gln
ENST00000456676.7:c.1240G>C	ENSP00000416687.3:p.Glu414Gln
ENST00000458009.6:c.*141G>C	ENSP00000411066.2:n.*141G>C
ENST00000492474.6:c.517G>C	ENSP00000518393.1:p.Glu173Gln
ENST00000616768.6:c.1240G>C	ENSP00000480669.3:p.Glu414Gln
ENST00000673673.2:c.1240G>C	ENSP00000500979.2:p.Glu414Gln
ENST00000231790.8:c.1240G>C MANE Select	ENSP00000231790.3:p.Glu414Gln
ENST00000413212.2:c.*158G>C	ENSP00000400844.2:n.*158G>C
ENST00000432299.6:c.*1072G>C	ENSP00000416783.1:n.*1072G>C
ENST00000441265.6:c.517G>C	ENSP00000398392.2:p.Glu173Gln
ENST00000442249.6:n.1048G>C
ENST00000447829.6:c.*351G>C	ENSP00000399329.2:n.*351G>C
ENST00000539477.6:c.517G>C	ENSP00000443665.1:p.Glu173Gln
ENST00000616768.5:c.277G>C	ENSP00000480669.2:p.Glu93Gln
ENST00000673673.1:c.1193G>C
ENST00000673713.1:n.1364G>C
ENST00000673715.1:c.1240G>C	ENSP00000501301.1:p.Glu414Gln
ENST00000673889.1:n.622G>C
ENST00000673897.1:c.*1032G>C	ENSP00000501109.1:n.*1032G>C
ENST00000673899.1:c.678-2946G>C	ENSP00000501030.1:n.678-2946G>C
ENST00000673947.1:c.*1380G>C	ENSP00000501304.1:n.*1380G>C
ENST00000673972.1:c.*1118G>C	ENSP00000501281.1:n.*1118G>C
ENST00000673990.1:n.1131G>C
ENST00000674019.1:c.517G>C	ENSP00000501081.1:p.Glu173Gln
ENST00000674107.1:n.1088G>C
ENST00000674111.1:c.1240G>C	ENSP00000501162.1:p.Glu414Gln
ENST00000231790.6:c.1240G>C	ENSP00000231790.2:p.Glu414Gln
ENST00000413212.1:c.315G>C
ENST00000435176.5:c.946G>C	ENSP00000402564.1:p.Glu316Gln
ENST00000447829.5:c.527G>C
ENST00000455445.6:c.517G>C	ENSP00000398272.2:p.Glu173Gln
ENST00000456676.6:c.1215G>C
ENST00000458009.5:c.427G>C
ENST00000458205.6:c.517G>C	ENSP00000402667.2:p.Glu173Gln
ENST00000536378.5:c.517G>C	ENSP00000444286.2:p.Glu173Gln
ENST00000539477.5:c.517G>C	ENSP00000443665.1:p.Glu173Gln
ENST00000616768.4:c.8G>C
NM_000249.3:c.1240G>C , LRG_216t1:c.1240G>C	NP_000240.1:p.Glu414Gln
NM_001167617.1:c.946G>C	NP_001161089.1:p.Glu316Gln
NM_001167618.1:c.517G>C	NP_001161090.1:p.Glu173Gln
NM_001167619.1:c.517G>C	NP_001161091.1:p.Glu173Gln
NM_001258271.1:c.1240G>C	NP_001245200.1:p.Glu414Gln
NM_001258273.1:c.517G>C	NP_001245202.1:p.Glu173Gln
NM_001258274.1:c.517G>C	NP_001245203.1:p.Glu173Gln
XM_005265161.1:c.1033G>C	XP_005265218.1:p.Glu345Gln
XM_005265163.1:c.517G>C	XP_005265220.1:p.Glu173Gln
XM_005265164.1:c.517G>C	XP_005265221.1:p.Glu173Gln
XM_005265166.1:c.217G>C	XP_005265223.1:p.Glu73Gln
XM_011533727.1:c.166G>C	XP_011532029.1:p.Glu56Gln
NM_001167617.2:c.946G>C	NP_001161089.1:p.Glu316Gln
NM_001167618.2:c.517G>C	NP_001161090.1:p.Glu173Gln
NM_001167619.2:c.517G>C	NP_001161091.1:p.Glu173Gln
NM_001258274.2:c.517G>C	NP_001245203.1:p.Glu173Gln
NM_001354615.1:c.517G>C	NP_001341544.1:p.Glu173Gln
NM_001354616.1:c.517G>C	NP_001341545.1:p.Glu173Gln
NM_001354617.1:c.517G>C	NP_001341546.1:p.Glu173Gln
NM_001354618.1:c.517G>C	NP_001341547.1:p.Glu173Gln
NM_001354619.1:c.517G>C	NP_001341548.1:p.Glu173Gln
NM_001354620.1:c.946G>C	NP_001341549.1:p.Glu316Gln
NM_001354621.1:c.217G>C	NP_001341550.1:p.Glu73Gln
NM_001354622.1:c.217G>C	NP_001341551.1:p.Glu73Gln
NM_001354623.1:c.217G>C	NP_001341552.1:p.Glu73Gln
NM_001354624.1:c.166G>C	NP_001341553.1:p.Glu56Gln
NM_001354625.1:c.166G>C	NP_001341554.1:p.Glu56Gln
NM_001354626.1:c.166G>C	NP_001341555.1:p.Glu56Gln
NM_001354627.1:c.166G>C	NP_001341556.1:p.Glu56Gln
NM_001354628.1:c.1240G>C	NP_001341557.1:p.Glu414Gln
NM_001354629.1:c.1141G>C	NP_001341558.1:p.Glu381Gln
NM_001354630.1:c.1240G>C	NP_001341559.1:p.Glu414Gln
XM_005265161.2:c.1033G>C	XP_005265218.1:p.Glu345Gln
XM_017006450.2:c.217G>C	XP_016861939.1:p.Glu73Gln
NM_000249.4:c.1240G>C MANE Select	NP_000240.1:p.Glu414Gln
NM_001167617.3:c.946G>C	NP_001161089.1:p.Glu316Gln
NM_001167618.3:c.517G>C	NP_001161090.1:p.Glu173Gln
NM_001167619.3:c.517G>C	NP_001161091.1:p.Glu173Gln
NM_001258271.2:c.1240G>C	NP_001245200.1:p.Glu414Gln
NM_001258273.2:c.517G>C	NP_001245202.1:p.Glu173Gln
NM_001258274.3:c.517G>C	NP_001245203.1:p.Glu173Gln
NM_001354615.2:c.517G>C	NP_001341544.1:p.Glu173Gln
NM_001354616.2:c.517G>C	NP_001341545.1:p.Glu173Gln
NM_001354617.2:c.517G>C	NP_001341546.1:p.Glu173Gln
NM_001354618.2:c.517G>C	NP_001341547.1:p.Glu173Gln
NM_001354619.2:c.517G>C	NP_001341548.1:p.Glu173Gln
NM_001354620.2:c.946G>C	NP_001341549.1:p.Glu316Gln
NM_001354621.2:c.217G>C	NP_001341550.1:p.Glu73Gln
NM_001354622.2:c.217G>C	NP_001341551.1:p.Glu73Gln
NM_001354623.2:c.217G>C	NP_001341552.1:p.Glu73Gln
NM_001354624.2:c.166G>C	NP_001341553.1:p.Glu56Gln
NM_001354625.2:c.166G>C	NP_001341554.1:p.Glu56Gln
NM_001354626.2:c.166G>C	NP_001341555.1:p.Glu56Gln
NM_001354627.2:c.166G>C	NP_001341556.1:p.Glu56Gln
NM_001354628.2:c.1240G>C	NP_001341557.1:p.Glu414Gln
NM_001354629.2:c.1141G>C	NP_001341558.1:p.Glu381Gln
NM_001354630.2:c.1240G>C	NP_001341559.1:p.Glu414Gln