Canonical Allele Identifier: CA2702257745
Gene: MLH1 HGNC NCBI

Linked Data

dbSNP Id: rs1057523910

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.36993667C>G , CM000665.2:g.36993667C>G GRCh38
NC_000003.11:g.37035158C>G , CM000665.1:g.37035158C>G GRCh37
NC_000003.10:g.37010162C>G NCBI36
NG_007109.2:g.5318C>G , LRG_216:g.5318C>G
NG_008418.1:g.4638G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000413740.2:c.116+4C>G ENSP00000416476.2:n.116+4C>G
ENST00000450420.6:c.116+4C>G ENSP00000393006.2:n.116+4C>G
ENST00000456676.7:c.116+4C>G ENSP00000416687.3:n.116+4C>G
ENST00000458009.6:c.116+4C>G ENSP00000411066.2:n.116+4C>G
ENST00000616768.6:c.116+4C>G ENSP00000480669.3:n.116+4C>G
ENST00000673673.2:c.116+4C>G ENSP00000500979.2:n.116+4C>G
ENST00000231790.8:c.116+4C>G MANE Select ENSP00000231790.3:n.116+4C>G
ENST00000432299.6:c.120C>G ENSP00000416783.1:p.Tyr40Ter
ENST00000442249.6:n.131+4C>G
ENST00000673673.1:c.69+4C>G
ENST00000673713.1:n.147+4C>G
ENST00000673715.1:c.116+4C>G ENSP00000501301.1:n.116+4C>G
ENST00000673897.1:c.116+4C>G ENSP00000501109.1:n.116+4C>G
ENST00000673899.1:c.116+4C>G ENSP00000501030.1:n.116+4C>G
ENST00000673947.1:c.116+4C>G ENSP00000501304.1:n.116+4C>G
ENST00000673972.1:c.116+4C>G ENSP00000501281.1:n.116+4C>G
ENST00000674111.1:c.116+4C>G ENSP00000501162.1:n.116+4C>G
ENST00000231790.6:c.116+4C>G ENSP00000231790.2:n.116+4C>G
ENST00000432299.5:c.120C>G ENSP00000416783.1:p.Tyr40Ter
ENST00000442249.5:c.116+4C>G ENSP00000387511.1:n.116+4C>G
ENST00000454028.5:c.116+4C>G ENSP00000392649.1:n.116+4C>G
ENST00000456676.6:c.91+4C>G
ENST00000457004.5:c.116+4C>G ENSP00000407773.1:n.116+4C>G
ENST00000536378.5:c.-517+4C>G ENSP00000444286.2:n.-517+4C>G
NM_000249.3:c.116+4C>G , LRG_216t1:c.116+4C>G NP_000240.1:n.116+4C>G
NM_001258271.1:c.116+4C>G NP_001245200.1:n.116+4C>G
NM_001258273.1:c.-517+4C>G NP_001245202.1:n.-517+4C>G
XM_005265161.1:c.116+4C>G XP_005265218.1:n.116+4C>G
XM_005265164.1:c.-603+4C>G XP_005265221.1:n.-603+4C>G
NM_001167617.2:c.-397C>G NP_001161089.1:n.-397C>G
NM_001167618.2:c.-826C>G NP_001161090.1:n.-826C>G
NM_001167619.2:c.-739C>G NP_001161091.1:n.-739C>G
NM_001258274.2:c.-976C>G NP_001245203.1:n.-976C>G
NM_001354615.1:c.-511+4C>G NP_001341544.1:n.-511+4C>G
NM_001354616.1:c.-511+4C>G NP_001341545.1:n.-511+4C>G
NM_001354617.1:c.-603+4C>G NP_001341546.1:n.-603+4C>G
NM_001354618.1:c.-831C>G NP_001341547.1:n.-831C>G
NM_001354619.1:c.-955C>G NP_001341548.1:n.-955C>G
NM_001354620.1:c.-169+4C>G NP_001341549.1:n.-169+4C>G
NM_001354621.1:c.-924C>G NP_001341550.1:n.-924C>G
NM_001354622.1:c.-1037C>G NP_001341551.1:n.-1037C>G
NM_001354623.1:c.-946C>G NP_001341552.1:n.-946C>G
NM_001354624.1:c.-711+4C>G NP_001341553.1:n.-711+4C>G
NM_001354625.1:c.-609+4C>G NP_001341554.1:n.-609+4C>G
NM_001354626.1:c.-706+4C>G NP_001341555.1:n.-706+4C>G
NM_001354627.1:c.-934C>G NP_001341556.1:n.-934C>G
NM_001354628.1:c.116+4C>G NP_001341557.1:n.116+4C>G
NM_001354629.1:c.116+4C>G NP_001341558.1:n.116+4C>G
NM_001354630.1:c.116+4C>G NP_001341559.1:n.116+4C>G
XM_005265161.2:c.116+4C>G XP_005265218.1:n.116+4C>G
XM_017006450.2:c.-696+4C>G XP_016861939.1:n.-696+4C>G
NM_000249.4:c.116+4C>G MANE Select NP_000240.1:n.116+4C>G
NM_001167617.3:c.-397C>G NP_001161089.1:n.-397C>G
NM_001167618.3:c.-826C>G NP_001161090.1:n.-826C>G
NM_001167619.3:c.-739C>G NP_001161091.1:n.-739C>G
NM_001258271.2:c.116+4C>G NP_001245200.1:n.116+4C>G
NM_001258273.2:c.-517+4C>G NP_001245202.1:n.-517+4C>G
NM_001258274.3:c.-976C>G NP_001245203.1:n.-976C>G
NM_001354615.2:c.-511+4C>G NP_001341544.1:n.-511+4C>G
NM_001354616.2:c.-511+4C>G NP_001341545.1:n.-511+4C>G
NM_001354617.2:c.-603+4C>G NP_001341546.1:n.-603+4C>G
NM_001354618.2:c.-831C>G NP_001341547.1:n.-831C>G
NM_001354619.2:c.-955C>G NP_001341548.1:n.-955C>G
NM_001354620.2:c.-169+4C>G NP_001341549.1:n.-169+4C>G
NM_001354621.2:c.-924C>G NP_001341550.1:n.-924C>G
NM_001354622.2:c.-1037C>G NP_001341551.1:n.-1037C>G
NM_001354623.2:c.-946C>G NP_001341552.1:n.-946C>G
NM_001354624.2:c.-711+4C>G NP_001341553.1:n.-711+4C>G
NM_001354625.2:c.-609+4C>G NP_001341554.1:n.-609+4C>G
NM_001354626.2:c.-706+4C>G NP_001341555.1:n.-706+4C>G
NM_001354627.2:c.-934C>G NP_001341556.1:n.-934C>G
NM_001354628.2:c.116+4C>G NP_001341557.1:n.116+4C>G
NM_001354629.2:c.116+4C>G NP_001341558.1:n.116+4C>G
NM_001354630.2:c.116+4C>G NP_001341559.1:n.116+4C>G