Canonical Allele Identifier: CA1357864883
Gene: MLH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.36993636A= , CM000665.2:g.36993636A= GRCh38
NC_000003.11:g.37035127A= , CM000665.1:g.37035127A= GRCh37
NC_000003.10:g.37010131A= NCBI36
NG_007109.2:g.5287A= , LRG_216:g.5287A=
NG_008418.1:g.4669T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000413740.2:c.89A= ENSP00000416476.2:p.Asn30=
ENST00000450420.6:c.89A= ENSP00000393006.2:p.Asn30=
ENST00000456676.7:c.89A= ENSP00000416687.3:p.Asn30=
ENST00000458009.6:c.89A= ENSP00000411066.2:p.Asn30=
ENST00000616768.6:c.89A= ENSP00000480669.3:p.Asn30=
ENST00000673673.2:c.89A= ENSP00000500979.2:p.Asn30=
ENST00000231790.8:c.89A= MANE Select ENSP00000231790.3:p.Asn30=
ENST00000432299.6:c.89A= ENSP00000416783.1:p.Asn30=
ENST00000442249.6:n.104A=
ENST00000673673.1:c.42A=
ENST00000673713.1:n.120A=
ENST00000673715.1:c.89A= ENSP00000501301.1:p.Asn30=
ENST00000673897.1:c.89A= ENSP00000501109.1:p.Asn30=
ENST00000673899.1:c.89A= ENSP00000501030.1:p.Asn30=
ENST00000673947.1:c.89A= ENSP00000501304.1:p.Asn30=
ENST00000673972.1:c.89A= ENSP00000501281.1:p.Asn30=
ENST00000674111.1:c.89A= ENSP00000501162.1:p.Asn30=
ENST00000231790.6:c.89A= ENSP00000231790.2:p.Asn30=
ENST00000432299.5:c.89A= ENSP00000416783.1:p.Asn30=
ENST00000442249.5:c.89A= ENSP00000387511.1:p.Asn30=
ENST00000454028.5:c.89A= ENSP00000392649.1:p.Asn30=
ENST00000456676.6:c.64A=
ENST00000457004.5:c.89A= ENSP00000407773.1:p.Asn30=
ENST00000536378.5:c.-544A= ENSP00000444286.2:n.-544A=
NM_000249.3:c.89A= , LRG_216t1:c.89A= NP_000240.1:p.Asn30=
NM_001258271.1:c.89A= NP_001245200.1:p.Asn30=
NM_001258273.1:c.-544A= NP_001245202.1:n.-544A=
XM_005265161.1:c.89A= XP_005265218.1:p.Asn30=
XM_005265164.1:c.-630A= XP_005265221.1:n.-630A=
NM_001167617.2:c.-428A= NP_001161089.1:n.-428A=
NM_001167618.2:c.-857A= NP_001161090.1:n.-857A=
NM_001167619.2:c.-770A= NP_001161091.1:n.-770A=
NM_001258274.2:c.-1007A= NP_001245203.1:n.-1007A=
NM_001354615.1:c.-538A= NP_001341544.1:n.-538A=
NM_001354616.1:c.-538A= NP_001341545.1:n.-538A=
NM_001354617.1:c.-630A= NP_001341546.1:n.-630A=
NM_001354618.1:c.-862A= NP_001341547.1:n.-862A=
NM_001354619.1:c.-986A= NP_001341548.1:n.-986A=
NM_001354620.1:c.-196A= NP_001341549.1:n.-196A=
NM_001354621.1:c.-955A= NP_001341550.1:n.-955A=
NM_001354622.1:c.-1068A= NP_001341551.1:n.-1068A=
NM_001354623.1:c.-977A= NP_001341552.1:n.-977A=
NM_001354624.1:c.-738A= NP_001341553.1:n.-738A=
NM_001354625.1:c.-636A= NP_001341554.1:n.-636A=
NM_001354626.1:c.-733A= NP_001341555.1:n.-733A=
NM_001354627.1:c.-965A= NP_001341556.1:n.-965A=
NM_001354628.1:c.89A= NP_001341557.1:p.Asn30=
NM_001354629.1:c.89A= NP_001341558.1:p.Asn30=
NM_001354630.1:c.89A= NP_001341559.1:p.Asn30=
XM_005265161.2:c.89A= XP_005265218.1:p.Asn30=
XM_017006450.2:c.-723A= XP_016861939.1:n.-723A=
NM_000249.4:c.89A= MANE Select NP_000240.1:p.Asn30=
NM_001167617.3:c.-428A= NP_001161089.1:n.-428A=
NM_001167618.3:c.-857A= NP_001161090.1:n.-857A=
NM_001167619.3:c.-770A= NP_001161091.1:n.-770A=
NM_001258271.2:c.89A= NP_001245200.1:p.Asn30=
NM_001258273.2:c.-544A= NP_001245202.1:n.-544A=
NM_001258274.3:c.-1007A= NP_001245203.1:n.-1007A=
NM_001354615.2:c.-538A= NP_001341544.1:n.-538A=
NM_001354616.2:c.-538A= NP_001341545.1:n.-538A=
NM_001354617.2:c.-630A= NP_001341546.1:n.-630A=
NM_001354618.2:c.-862A= NP_001341547.1:n.-862A=
NM_001354619.2:c.-986A= NP_001341548.1:n.-986A=
NM_001354620.2:c.-196A= NP_001341549.1:n.-196A=
NM_001354621.2:c.-955A= NP_001341550.1:n.-955A=
NM_001354622.2:c.-1068A= NP_001341551.1:n.-1068A=
NM_001354623.2:c.-977A= NP_001341552.1:n.-977A=
NM_001354624.2:c.-738A= NP_001341553.1:n.-738A=
NM_001354625.2:c.-636A= NP_001341554.1:n.-636A=
NM_001354626.2:c.-733A= NP_001341555.1:n.-733A=
NM_001354627.2:c.-965A= NP_001341556.1:n.-965A=
NM_001354628.2:c.89A= NP_001341557.1:p.Asn30=
NM_001354629.2:c.89A= NP_001341558.1:p.Asn30=
NM_001354630.2:c.89A= NP_001341559.1:p.Asn30=