Canonical Allele Identifier: CA352060980
Gene: MLH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 629311
dbSNP Id: rs63750216

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.36993633C>A , CM000665.2:g.36993633C>A GRCh38
NC_000003.11:g.37035124C>A , CM000665.1:g.37035124C>A GRCh37
NC_000003.10:g.37010128C>A NCBI36
NG_007109.2:g.5284C>A , LRG_216:g.5284C>A
NG_008418.1:g.4672G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000413740.2:c.86C>A ENSP00000416476.2:p.Ala29Asp
ENST00000450420.6:c.86C>A ENSP00000393006.2:p.Ala29Asp
ENST00000456676.7:c.86C>A ENSP00000416687.3:p.Ala29Asp
ENST00000458009.6:c.86C>A ENSP00000411066.2:p.Ala29Asp
ENST00000616768.6:c.86C>A ENSP00000480669.3:p.Ala29Asp
ENST00000673673.2:c.86C>A ENSP00000500979.2:p.Ala29Asp
ENST00000231790.8:c.86C>A MANE Select ENSP00000231790.3:p.Ala29Asp
ENST00000432299.6:c.86C>A ENSP00000416783.1:p.Ala29Asp
ENST00000442249.6:n.101C>A
ENST00000673673.1:c.39C>A
ENST00000673713.1:n.117C>A
ENST00000673715.1:c.86C>A ENSP00000501301.1:p.Ala29Asp
ENST00000673897.1:c.86C>A ENSP00000501109.1:p.Ala29Asp
ENST00000673899.1:c.86C>A ENSP00000501030.1:p.Ala29Asp
ENST00000673947.1:c.86C>A ENSP00000501304.1:p.Ala29Asp
ENST00000673972.1:c.86C>A ENSP00000501281.1:p.Ala29Asp
ENST00000674111.1:c.86C>A ENSP00000501162.1:p.Ala29Asp
ENST00000231790.6:c.86C>A ENSP00000231790.2:p.Ala29Asp
ENST00000432299.5:c.86C>A ENSP00000416783.1:p.Ala29Asp
ENST00000442249.5:c.86C>A ENSP00000387511.1:p.Ala29Asp
ENST00000454028.5:c.86C>A ENSP00000392649.1:p.Ala29Asp
ENST00000456676.6:c.61C>A
ENST00000457004.5:c.86C>A ENSP00000407773.1:p.Ala29Asp
ENST00000536378.5:c.-547C>A ENSP00000444286.2:n.-547C>A
NM_000249.3:c.86C>A , LRG_216t1:c.86C>A NP_000240.1:p.Ala29Asp
NM_001258271.1:c.86C>A NP_001245200.1:p.Ala29Asp
NM_001258273.1:c.-547C>A NP_001245202.1:n.-547C>A
XM_005265161.1:c.86C>A XP_005265218.1:p.Ala29Asp
XM_005265164.1:c.-633C>A XP_005265221.1:n.-633C>A
NM_001167617.2:c.-431C>A NP_001161089.1:n.-431C>A
NM_001167618.2:c.-860C>A NP_001161090.1:n.-860C>A
NM_001167619.2:c.-773C>A NP_001161091.1:n.-773C>A
NM_001258274.2:c.-1010C>A NP_001245203.1:n.-1010C>A
NM_001354615.1:c.-541C>A NP_001341544.1:n.-541C>A
NM_001354616.1:c.-541C>A NP_001341545.1:n.-541C>A
NM_001354617.1:c.-633C>A NP_001341546.1:n.-633C>A
NM_001354618.1:c.-865C>A NP_001341547.1:n.-865C>A
NM_001354619.1:c.-989C>A NP_001341548.1:n.-989C>A
NM_001354620.1:c.-199C>A NP_001341549.1:n.-199C>A
NM_001354621.1:c.-958C>A NP_001341550.1:n.-958C>A
NM_001354622.1:c.-1071C>A NP_001341551.1:n.-1071C>A
NM_001354623.1:c.-980C>A NP_001341552.1:n.-980C>A
NM_001354624.1:c.-741C>A NP_001341553.1:n.-741C>A
NM_001354625.1:c.-639C>A NP_001341554.1:n.-639C>A
NM_001354626.1:c.-736C>A NP_001341555.1:n.-736C>A
NM_001354627.1:c.-968C>A NP_001341556.1:n.-968C>A
NM_001354628.1:c.86C>A NP_001341557.1:p.Ala29Asp
NM_001354629.1:c.86C>A NP_001341558.1:p.Ala29Asp
NM_001354630.1:c.86C>A NP_001341559.1:p.Ala29Asp
XM_005265161.2:c.86C>A XP_005265218.1:p.Ala29Asp
XM_017006450.2:c.-726C>A XP_016861939.1:n.-726C>A
NM_000249.4:c.86C>A MANE Select NP_000240.1:p.Ala29Asp
NM_001167617.3:c.-431C>A NP_001161089.1:n.-431C>A
NM_001167618.3:c.-860C>A NP_001161090.1:n.-860C>A
NM_001167619.3:c.-773C>A NP_001161091.1:n.-773C>A
NM_001258271.2:c.86C>A NP_001245200.1:p.Ala29Asp
NM_001258273.2:c.-547C>A NP_001245202.1:n.-547C>A
NM_001258274.3:c.-1010C>A NP_001245203.1:n.-1010C>A
NM_001354615.2:c.-541C>A NP_001341544.1:n.-541C>A
NM_001354616.2:c.-541C>A NP_001341545.1:n.-541C>A
NM_001354617.2:c.-633C>A NP_001341546.1:n.-633C>A
NM_001354618.2:c.-865C>A NP_001341547.1:n.-865C>A
NM_001354619.2:c.-989C>A NP_001341548.1:n.-989C>A
NM_001354620.2:c.-199C>A NP_001341549.1:n.-199C>A
NM_001354621.2:c.-958C>A NP_001341550.1:n.-958C>A
NM_001354622.2:c.-1071C>A NP_001341551.1:n.-1071C>A
NM_001354623.2:c.-980C>A NP_001341552.1:n.-980C>A
NM_001354624.2:c.-741C>A NP_001341553.1:n.-741C>A
NM_001354625.2:c.-639C>A NP_001341554.1:n.-639C>A
NM_001354626.2:c.-736C>A NP_001341555.1:n.-736C>A
NM_001354627.2:c.-968C>A NP_001341556.1:n.-968C>A
NM_001354628.2:c.86C>A NP_001341557.1:p.Ala29Asp
NM_001354629.2:c.86C>A NP_001341558.1:p.Ala29Asp
NM_001354630.2:c.86C>A NP_001341559.1:p.Ala29Asp