Canonical Allele Identifier: CA352067611
Gene: MLH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.37048910T>G , CM000665.2:g.37048910T>G GRCh38
NC_000003.11:g.37090401T>G , CM000665.1:g.37090401T>G GRCh37
NC_000003.10:g.37065405T>G NCBI36
NG_007109.2:g.60561T>G , LRG_216:g.60561T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000413740.2:c.1668-1576T>G ENSP00000416476.2:n.1668-1576T>G
ENST00000429117.6:c.1702T>G ENSP00000407019.2:p.Trp568Gly
ENST00000450420.6:c.1559-1576T>G ENSP00000393006.2:n.1559-1576T>G
ENST00000456676.7:c.1896+1227T>G ENSP00000416687.3:n.1896+1227T>G
ENST00000492474.6:c.1273T>G ENSP00000518393.1:p.Trp425Gly
ENST00000616768.6:c.1903T>G ENSP00000480669.3:p.Trp635Gly
ENST00000673673.2:c.1831T>G ENSP00000500979.2:p.Trp611Gly
ENST00000231790.8:c.1996T>G MANE Select ENSP00000231790.3:p.Trp666Gly
ENST00000413212.2:c.*914T>G ENSP00000400844.2:n.*914T>G
ENST00000432299.6:c.*1828T>G ENSP00000416783.1:n.*1828T>G
ENST00000447829.6:c.*1107T>G ENSP00000399329.2:n.*1107T>G
ENST00000539477.6:c.1273T>G ENSP00000443665.1:p.Trp425Gly
ENST00000616768.5:c.940T>G ENSP00000480669.2:p.Trp314Gly
ENST00000673673.1:c.1784T>G
ENST00000673741.1:n.1030T>G
ENST00000673889.1:n.1378T>G
ENST00000673897.1:c.*1788T>G ENSP00000501109.1:n.*1788T>G
ENST00000673899.1:c.1264T>G ENSP00000501030.1:p.Trp422Gly
ENST00000673947.1:c.*2136T>G ENSP00000501304.1:n.*2136T>G
ENST00000673972.1:c.*1874T>G ENSP00000501281.1:n.*1874T>G
ENST00000674019.1:c.1273T>G ENSP00000501081.1:p.Trp425Gly
ENST00000674111.1:c.*225T>G ENSP00000501162.1:n.*225T>G
ENST00000674125.1:n.707T>G
ENST00000231790.6:c.1996T>G ENSP00000231790.2:p.Trp666Gly
ENST00000413740.1:c.291-1576T>G ENSP00000416476.1:n.291-1576T>G
ENST00000435176.5:c.1702T>G ENSP00000402564.1:p.Trp568Gly
ENST00000450420.5:c.182-1576T>G ENSP00000393006.1:n.182-1576T>G
ENST00000455445.6:c.1273T>G ENSP00000398272.2:p.Trp425Gly
ENST00000456676.6:c.1871+1227T>G
ENST00000458205.6:c.1273T>G ENSP00000402667.2:p.Trp425Gly
ENST00000536378.5:c.1273T>G ENSP00000444286.2:p.Trp425Gly
ENST00000539477.5:c.1273T>G ENSP00000443665.1:p.Trp425Gly
NM_000249.3:c.1996T>G , LRG_216t1:c.1996T>G NP_000240.1:p.Trp666Gly
NM_001167617.1:c.1702T>G NP_001161089.1:p.Trp568Gly
NM_001167618.1:c.1273T>G NP_001161090.1:p.Trp425Gly
NM_001167619.1:c.1273T>G NP_001161091.1:p.Trp425Gly
NM_001258271.1:c.1896+1227T>G NP_001245200.1:n.1896+1227T>G
NM_001258273.1:c.1273T>G NP_001245202.1:p.Trp425Gly
NM_001258274.1:c.1273T>G NP_001245203.1:p.Trp425Gly
XM_005265161.1:c.1789T>G XP_005265218.1:p.Trp597Gly
XM_005265163.1:c.1273T>G XP_005265220.1:p.Trp425Gly
XM_005265164.1:c.1273T>G XP_005265221.1:p.Trp425Gly
XM_005265166.1:c.973T>G XP_005265223.1:p.Trp325Gly
XM_011533727.1:c.922T>G XP_011532029.1:p.Trp308Gly
NM_001167617.2:c.1702T>G NP_001161089.1:p.Trp568Gly
NM_001167618.2:c.1273T>G NP_001161090.1:p.Trp425Gly
NM_001167619.2:c.1273T>G NP_001161091.1:p.Trp425Gly
NM_001258274.2:c.1273T>G NP_001245203.1:p.Trp425Gly
NM_001354615.1:c.1273T>G NP_001341544.1:p.Trp425Gly
NM_001354616.1:c.1273T>G NP_001341545.1:p.Trp425Gly
NM_001354617.1:c.1273T>G NP_001341546.1:p.Trp425Gly
NM_001354618.1:c.1273T>G NP_001341547.1:p.Trp425Gly
NM_001354619.1:c.1273T>G NP_001341548.1:p.Trp425Gly
NM_001354620.1:c.1702T>G NP_001341549.1:p.Trp568Gly
NM_001354621.1:c.973T>G NP_001341550.1:p.Trp325Gly
NM_001354622.1:c.973T>G NP_001341551.1:p.Trp325Gly
NM_001354623.1:c.973T>G NP_001341552.1:p.Trp325Gly
NM_001354624.1:c.922T>G NP_001341553.1:p.Trp308Gly
NM_001354625.1:c.922T>G NP_001341554.1:p.Trp308Gly
NM_001354626.1:c.922T>G NP_001341555.1:p.Trp308Gly
NM_001354627.1:c.922T>G NP_001341556.1:p.Trp308Gly
NM_001354628.1:c.1903T>G NP_001341557.1:p.Trp635Gly
NM_001354629.1:c.1897T>G NP_001341558.1:p.Trp633Gly
NM_001354630.1:c.1831T>G NP_001341559.1:p.Trp611Gly
XM_005265161.2:c.1789T>G XP_005265218.1:p.Trp597Gly
XM_017006450.2:c.973T>G XP_016861939.1:p.Trp325Gly
NM_000249.4:c.1996T>G MANE Select NP_000240.1:p.Trp666Gly
NM_001167617.3:c.1702T>G NP_001161089.1:p.Trp568Gly
NM_001167618.3:c.1273T>G NP_001161090.1:p.Trp425Gly
NM_001167619.3:c.1273T>G NP_001161091.1:p.Trp425Gly
NM_001258271.2:c.1896+1227T>G NP_001245200.1:n.1896+1227T>G
NM_001258273.2:c.1273T>G NP_001245202.1:p.Trp425Gly
NM_001258274.3:c.1273T>G NP_001245203.1:p.Trp425Gly
NM_001354615.2:c.1273T>G NP_001341544.1:p.Trp425Gly
NM_001354616.2:c.1273T>G NP_001341545.1:p.Trp425Gly
NM_001354617.2:c.1273T>G NP_001341546.1:p.Trp425Gly
NM_001354618.2:c.1273T>G NP_001341547.1:p.Trp425Gly
NM_001354619.2:c.1273T>G NP_001341548.1:p.Trp425Gly
NM_001354620.2:c.1702T>G NP_001341549.1:p.Trp568Gly
NM_001354621.2:c.973T>G NP_001341550.1:p.Trp325Gly
NM_001354622.2:c.973T>G NP_001341551.1:p.Trp325Gly
NM_001354623.2:c.973T>G NP_001341552.1:p.Trp325Gly
NM_001354624.2:c.922T>G NP_001341553.1:p.Trp308Gly
NM_001354625.2:c.922T>G NP_001341554.1:p.Trp308Gly
NM_001354626.2:c.922T>G NP_001341555.1:p.Trp308Gly
NM_001354627.2:c.922T>G NP_001341556.1:p.Trp308Gly
NM_001354628.2:c.1903T>G NP_001341557.1:p.Trp635Gly
NM_001354629.2:c.1897T>G NP_001341558.1:p.Trp633Gly
NM_001354630.2:c.1831T>G NP_001341559.1:p.Trp611Gly