Canonical Allele Identifier: CA005617
Gene: MLH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 89756
ClinVar RCV Id: RCV000075230
dbSNP Id: rs63749956

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.36996652dup , CM000665.2:g.36996652dup GRCh38
NC_000003.11:g.37038143dup , CM000665.1:g.37038143dup GRCh37
NC_000003.10:g.37013147dup NCBI36
NG_007109.2:g.8303dup , LRG_216:g.8303dup
NG_008418.1:g.1654dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000413740.2:c.150dup ENSP00000416476.2:p.Val51CysfsTer2
ENST00000429117.6:c.-140dup ENSP00000407019.2:n.-140dup
ENST00000450420.6:c.150dup ENSP00000393006.2:p.Val51CysfsTer2
ENST00000456676.7:c.150dup ENSP00000416687.3:p.Val51CysfsTer2
ENST00000458009.6:c.150dup ENSP00000411066.2:p.Val51CysfsTer2
ENST00000492474.6:c.-574dup ENSP00000518393.1:n.-574dup
ENST00000616768.6:c.150dup ENSP00000480669.3:p.Val51CysfsTer2
ENST00000673673.2:c.150dup ENSP00000500979.2:p.Val51CysfsTer2
ENST00000231790.8:c.150dup MANE Select ENSP00000231790.3:p.Val51CysfsTer2
ENST00000413212.2:c.-574dup ENSP00000400844.2:n.-574dup
ENST00000432299.6:c.*230dup ENSP00000416783.1:n.*230dup
ENST00000441265.6:c.-574dup ENSP00000398392.2:n.-574dup
ENST00000442249.6:n.165dup
ENST00000447829.6:c.-140dup ENSP00000399329.2:n.-140dup
ENST00000476172.6:n.1120-1318dup
ENST00000539477.6:c.-482dup ENSP00000443665.1:n.-482dup
ENST00000673673.1:c.103dup
ENST00000673686.1:n.140dup
ENST00000673713.1:n.181dup
ENST00000673715.1:c.150dup ENSP00000501301.1:p.Val51CysfsTer2
ENST00000673897.1:c.116+2989dup ENSP00000501109.1:n.116+2989dup
ENST00000673899.1:c.150dup ENSP00000501030.1:p.Val51CysfsTer2
ENST00000673947.1:c.*290dup ENSP00000501304.1:n.*290dup
ENST00000673972.1:c.*28dup ENSP00000501281.1:n.*28dup
ENST00000673990.1:n.135dup
ENST00000674019.1:c.-574dup ENSP00000501081.1:n.-574dup
ENST00000674107.1:n.92dup
ENST00000674111.1:c.150dup ENSP00000501162.1:p.Val51CysfsTer2
ENST00000231790.6:c.150dup ENSP00000231790.2:p.Val51CysfsTer2
ENST00000429117.5:c.-140dup ENSP00000407019.1:n.-140dup
ENST00000432299.5:c.*230dup ENSP00000416783.1:n.*230dup
ENST00000435176.5:c.-140dup ENSP00000402564.1:n.-140dup
ENST00000441265.5:c.-482dup ENSP00000398392.1:n.-482dup
ENST00000442249.5:c.116+2989dup ENSP00000387511.1:n.116+2989dup
ENST00000454028.5:c.*28dup ENSP00000392649.1:n.*28dup
ENST00000455445.6:c.-574dup ENSP00000398272.2:n.-574dup
ENST00000456676.6:c.125dup
ENST00000457004.5:c.*28dup ENSP00000407773.1:n.*28dup
ENST00000458205.6:c.-719dup ENSP00000402667.2:n.-719dup
ENST00000466900.5:n.77dup
ENST00000476172.5:n.272dup
ENST00000485889.1:n.154dup
ENST00000492474.5:n.173dup
ENST00000536378.5:c.-517+2989dup ENSP00000444286.2:n.-517+2989dup
ENST00000539477.5:c.-482dup ENSP00000443665.1:n.-482dup
NM_000249.3:c.150dup , LRG_216t1:c.150dup NP_000240.1:p.Val51CysfsTer2
NM_001167617.1:c.-140dup NP_001161089.1:n.-140dup
NM_001167618.1:c.-574dup NP_001161090.1:n.-574dup
NM_001167619.1:c.-482dup NP_001161091.1:n.-482dup
NM_001258271.1:c.150dup NP_001245200.1:p.Val51CysfsTer2
NM_001258273.1:c.-517+2989dup NP_001245202.1:n.-517+2989dup
NM_001258274.1:c.-719dup NP_001245203.1:n.-719dup
XM_005265161.1:c.150dup XP_005265218.1:p.Val51CysfsTer2
XM_005265163.1:c.-574dup XP_005265220.1:n.-574dup
XM_005265164.1:c.-574dup XP_005265221.1:n.-574dup
XM_005265166.1:c.-780dup XP_005265223.1:n.-780dup
XM_011533727.1:c.-677dup XP_011532029.1:n.-677dup
NM_001167617.2:c.-140dup NP_001161089.1:n.-140dup
NM_001167618.2:c.-574dup NP_001161090.1:n.-574dup
NM_001167619.2:c.-482dup NP_001161091.1:n.-482dup
NM_001258274.2:c.-719dup NP_001245203.1:n.-719dup
NM_001354615.1:c.-477dup NP_001341544.1:n.-477dup
NM_001354616.1:c.-482dup NP_001341545.1:n.-482dup
NM_001354617.1:c.-574dup NP_001341546.1:n.-574dup
NM_001354618.1:c.-574dup NP_001341547.1:n.-574dup
NM_001354619.1:c.-574dup NP_001341548.1:n.-574dup
NM_001354620.1:c.-140dup NP_001341549.1:n.-140dup
NM_001354621.1:c.-667dup NP_001341550.1:n.-667dup
NM_001354622.1:c.-780dup NP_001341551.1:n.-780dup
NM_001354623.1:c.-723+2762dup NP_001341552.1:n.-723+2762dup
NM_001354624.1:c.-677dup NP_001341553.1:n.-677dup
NM_001354625.1:c.-580dup NP_001341554.1:n.-580dup
NM_001354626.1:c.-677dup NP_001341555.1:n.-677dup
NM_001354627.1:c.-677dup NP_001341556.1:n.-677dup
NM_001354628.1:c.150dup NP_001341557.1:p.Val51CysfsTer2
NM_001354629.1:c.150dup NP_001341558.1:p.Val51CysfsTer2
NM_001354630.1:c.150dup NP_001341559.1:p.Val51CysfsTer2
XM_005265161.2:c.150dup XP_005265218.1:p.Val51CysfsTer2
XM_017006450.2:c.-667dup XP_016861939.1:n.-667dup
NM_000249.4:c.150dup MANE Select NP_000240.1:p.Val51CysfsTer2
NM_001167617.3:c.-140dup NP_001161089.1:n.-140dup
NM_001167618.3:c.-574dup NP_001161090.1:n.-574dup
NM_001167619.3:c.-482dup NP_001161091.1:n.-482dup
NM_001258271.2:c.150dup NP_001245200.1:p.Val51CysfsTer2
NM_001258273.2:c.-517+2989dup NP_001245202.1:n.-517+2989dup
NM_001258274.3:c.-719dup NP_001245203.1:n.-719dup
NM_001354615.2:c.-477dup NP_001341544.1:n.-477dup
NM_001354616.2:c.-482dup NP_001341545.1:n.-482dup
NM_001354617.2:c.-574dup NP_001341546.1:n.-574dup
NM_001354618.2:c.-574dup NP_001341547.1:n.-574dup
NM_001354619.2:c.-574dup NP_001341548.1:n.-574dup
NM_001354620.2:c.-140dup NP_001341549.1:n.-140dup
NM_001354621.2:c.-667dup NP_001341550.1:n.-667dup
NM_001354622.2:c.-780dup NP_001341551.1:n.-780dup
NM_001354623.2:c.-723+2762dup NP_001341552.1:n.-723+2762dup
NM_001354624.2:c.-677dup NP_001341553.1:n.-677dup
NM_001354625.2:c.-580dup NP_001341554.1:n.-580dup
NM_001354626.2:c.-677dup NP_001341555.1:n.-677dup
NM_001354627.2:c.-677dup NP_001341556.1:n.-677dup
NM_001354628.2:c.150dup NP_001341557.1:p.Val51CysfsTer2
NM_001354629.2:c.150dup NP_001341558.1:p.Val51CysfsTer2
NM_001354630.2:c.150dup NP_001341559.1:p.Val51CysfsTer2