Canonical Allele Identifier: CA004476
Gene: MLH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 89651
ClinVar RCV Id: RCV000075121
dbSNP Id: rs267607706

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.36993661C>G , CM000665.2:g.36993661C>G GRCh38
NC_000003.11:g.37035152C>G , CM000665.1:g.37035152C>G GRCh37
NC_000003.10:g.37010156C>G NCBI36
NG_007109.2:g.5312C>G , LRG_216:g.5312C>G
NG_008418.1:g.4644G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000231790.8:c.114C>G MANE Select ENSP00000231790.3:p.Asn38Lys
ENST00000432299.6:c.114C>G ENSP00000416783.1:p.Asn38Lys
ENST00000442249.6:n.129C>G
ENST00000673673.1:n.67C>G
ENST00000673713.1:n.145C>G
ENST00000673715.1:c.114C>G ENSP00000501301.1:p.Asn38Lys
ENST00000673897.1:c.114C>G ENSP00000501109.1:p.Asn38Lys
ENST00000673899.1:c.114C>G ENSP00000501030.1:p.Asn38Lys
ENST00000673947.1:c.114C>G ENSP00000501304.1:p.Asn38Lys
ENST00000673972.1:c.114C>G ENSP00000501281.1:p.Asn38Lys
ENST00000674111.1:c.114C>G ENSP00000501162.1:p.Asn38Lys
ENST00000231790.6:c.114C>G ENSP00000231790.2:p.Asn38Lys
ENST00000432299.5:c.114C>G ENSP00000416783.1:p.Asn38Lys
ENST00000442249.5:c.114C>G ENSP00000387511.1:p.Asn38Lys
ENST00000454028.5:c.114C>G ENSP00000392649.1:p.Asn38Lys
ENST00000456676.6:n.89C>G
ENST00000457004.5:c.114C>G ENSP00000407773.1:p.Asn38Lys
ENST00000536378.5:c.-519C>G ENSP00000444286.2:p.=
NM_000249.3:c.114C>G , LRG_216t1:c.114C>G NP_000240.1:p.Asn38Lys
NM_001258271.1:c.114C>G NP_001245200.1:p.Asn38Lys
NM_001258273.1:c.-519C>G NP_001245202.1:p.=
XM_005265161.1:c.114C>G XP_005265218.1:p.Asn38Lys
XM_005265164.1:c.-605C>G XP_005265221.1:p.=
NM_001167617.2:c.-403C>G NP_001161089.1:p.=
NM_001167618.2:c.-832C>G NP_001161090.1:p.=
NM_001167619.2:c.-745C>G NP_001161091.1:p.=
NM_001258274.2:c.-982C>G NP_001245203.1:p.=
NM_001354615.1:c.-513C>G NP_001341544.1:p.=
NM_001354616.1:c.-513C>G NP_001341545.1:p.=
NM_001354617.1:c.-605C>G NP_001341546.1:p.=
NM_001354618.1:c.-837C>G NP_001341547.1:p.=
NM_001354619.1:c.-961C>G NP_001341548.1:p.=
NM_001354620.1:c.-171C>G NP_001341549.1:p.=
NM_001354621.1:c.-930C>G NP_001341550.1:p.=
NM_001354622.1:c.-1043C>G NP_001341551.1:p.=
NM_001354623.1:c.-952C>G NP_001341552.1:p.=
NM_001354624.1:c.-713C>G NP_001341553.1:p.=
NM_001354625.1:c.-611C>G NP_001341554.1:p.=
NM_001354626.1:c.-708C>G NP_001341555.1:p.=
NM_001354627.1:c.-940C>G NP_001341556.1:p.=
NM_001354628.1:c.114C>G NP_001341557.1:p.Asn38Lys
NM_001354629.1:c.114C>G NP_001341558.1:p.Asn38Lys
NM_001354630.1:c.114C>G NP_001341559.1:p.Asn38Lys
XM_005265161.2:c.114C>G XP_005265218.1:p.Asn38Lys
XM_017006450.2:c.-698C>G XP_016861939.1:p.=
NM_000249.4:c.114C>G MANE Select NP_000240.1:p.Asn38Lys
NM_001167617.3:c.-403C>G NP_001161089.1:p.=
NM_001167618.3:c.-832C>G NP_001161090.1:p.=
NM_001167619.3:c.-745C>G NP_001161091.1:p.=
NM_001258271.2:c.114C>G NP_001245200.1:p.Asn38Lys
NM_001258273.2:c.-519C>G NP_001245202.1:p.=
NM_001258274.3:c.-982C>G NP_001245203.1:p.=
NM_001354615.2:c.-513C>G NP_001341544.1:p.=
NM_001354616.2:c.-513C>G NP_001341545.1:p.=
NM_001354617.2:c.-605C>G NP_001341546.1:p.=
NM_001354618.2:c.-837C>G NP_001341547.1:p.=
NM_001354619.2:c.-961C>G NP_001341548.1:p.=
NM_001354620.2:c.-171C>G NP_001341549.1:p.=
NM_001354621.2:c.-930C>G NP_001341550.1:p.=
NM_001354622.2:c.-1043C>G NP_001341551.1:p.=
NM_001354623.2:c.-952C>G NP_001341552.1:p.=
NM_001354624.2:c.-713C>G NP_001341553.1:p.=
NM_001354625.2:c.-611C>G NP_001341554.1:p.=
NM_001354626.2:c.-708C>G NP_001341555.1:p.=
NM_001354627.2:c.-940C>G NP_001341556.1:p.=
NM_001354628.2:c.114C>G NP_001341557.1:p.Asn38Lys
NM_001354629.2:c.114C>G NP_001341558.1:p.Asn38Lys
NM_001354630.2:c.114C>G NP_001341559.1:p.Asn38Lys