Canonical Allele Identifier: CA352060401

Gene: MLH1

Linked Data

• ClinVar Variation Id: 1723699
• ClinVar RCV Id: RCV002308973 ; RCV002400445
• dbSNP Id: rs1366752604
• gnomAD v2: 3-37035054-G-T
• gnomAD v3: 3-36993563-G-T
• gnomAD v4: 3-36993563-G-T
• MyVariant Identifiers: chr3:g.37035054G>T (hg19) ; chr3:g.36993563G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.36993563G>T , CM000665.2:g.36993563G>T	GRCh38
NC_000003.11:g.37035054G>T , CM000665.1:g.37035054G>T	GRCh37
NC_000003.10:g.37010058G>T	NCBI36
NG_007109.2:g.5214G>T , LRG_216:g.5214G>T
NG_008418.1:g.4742C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000413740.2:c.16G>T	ENSP00000416476.2:p.Gly6Trp
ENST00000450420.6:c.16G>T	ENSP00000393006.2:p.Gly6Trp
ENST00000456676.7:c.16G>T	ENSP00000416687.3:p.Gly6Trp
ENST00000458009.6:c.16G>T	ENSP00000411066.2:p.Gly6Trp
ENST00000616768.6:c.16G>T	ENSP00000480669.3:p.Gly6Trp
ENST00000673673.2:c.16G>T	ENSP00000500979.2:p.Gly6Trp
ENST00000231790.8:c.16G>T MANE Select	ENSP00000231790.3:p.Gly6Trp
ENST00000432299.6:c.16G>T	ENSP00000416783.1:p.Gly6Trp
ENST00000442249.6:n.31G>T
ENST00000673713.1:n.47G>T
ENST00000673715.1:c.16G>T	ENSP00000501301.1:p.Gly6Trp
ENST00000673897.1:c.16G>T	ENSP00000501109.1:p.Gly6Trp
ENST00000673899.1:c.16G>T	ENSP00000501030.1:p.Gly6Trp
ENST00000673947.1:c.16G>T	ENSP00000501304.1:p.Gly6Trp
ENST00000673972.1:c.16G>T	ENSP00000501281.1:p.Gly6Trp
ENST00000674111.1:c.16G>T	ENSP00000501162.1:p.Gly6Trp
ENST00000231790.6:c.16G>T	ENSP00000231790.2:p.Gly6Trp
ENST00000432299.5:c.16G>T	ENSP00000416783.1:p.Gly6Trp
ENST00000442249.5:c.16G>T	ENSP00000387511.1:p.Gly6Trp
ENST00000454028.5:c.16G>T	ENSP00000392649.1:p.Gly6Trp
ENST00000457004.5:c.16G>T	ENSP00000407773.1:p.Gly6Trp
ENST00000536378.5:c.-617G>T	ENSP00000444286.2:n.-617G>T
NM_000249.3:c.16G>T , LRG_216t1:c.16G>T	NP_000240.1:p.Gly6Trp
NM_001258271.1:c.16G>T	NP_001245200.1:p.Gly6Trp
NM_001258273.1:c.-617G>T	NP_001245202.1:n.-617G>T
XM_005265161.1:c.16G>T	XP_005265218.1:p.Gly6Trp
XM_005265164.1:c.-703G>T	XP_005265221.1:n.-703G>T
NM_001167617.2:c.-501G>T	NP_001161089.1:n.-501G>T
NM_001167618.2:c.-930G>T	NP_001161090.1:n.-930G>T
NM_001167619.2:c.-843G>T	NP_001161091.1:n.-843G>T
NM_001258274.2:c.-1080G>T	NP_001245203.1:n.-1080G>T
NM_001354615.1:c.-611G>T	NP_001341544.1:n.-611G>T
NM_001354616.1:c.-611G>T	NP_001341545.1:n.-611G>T
NM_001354617.1:c.-703G>T	NP_001341546.1:n.-703G>T
NM_001354618.1:c.-935G>T	NP_001341547.1:n.-935G>T
NM_001354619.1:c.-1059G>T	NP_001341548.1:n.-1059G>T
NM_001354620.1:c.-269G>T	NP_001341549.1:n.-269G>T
NM_001354621.1:c.-1028G>T	NP_001341550.1:n.-1028G>T
NM_001354622.1:c.-1141G>T	NP_001341551.1:n.-1141G>T
NM_001354623.1:c.-1050G>T	NP_001341552.1:n.-1050G>T
NM_001354624.1:c.-811G>T	NP_001341553.1:n.-811G>T
NM_001354625.1:c.-709G>T	NP_001341554.1:n.-709G>T
NM_001354626.1:c.-806G>T	NP_001341555.1:n.-806G>T
NM_001354627.1:c.-1038G>T	NP_001341556.1:n.-1038G>T
NM_001354628.1:c.16G>T	NP_001341557.1:p.Gly6Trp
NM_001354629.1:c.16G>T	NP_001341558.1:p.Gly6Trp
NM_001354630.1:c.16G>T	NP_001341559.1:p.Gly6Trp
XM_005265161.2:c.16G>T	XP_005265218.1:p.Gly6Trp
XM_017006450.2:c.-796G>T	XP_016861939.1:n.-796G>T
NM_000249.4:c.16G>T MANE Select	NP_000240.1:p.Gly6Trp
NM_001167617.3:c.-501G>T	NP_001161089.1:n.-501G>T
NM_001167618.3:c.-930G>T	NP_001161090.1:n.-930G>T
NM_001167619.3:c.-843G>T	NP_001161091.1:n.-843G>T
NM_001258271.2:c.16G>T	NP_001245200.1:p.Gly6Trp
NM_001258273.2:c.-617G>T	NP_001245202.1:n.-617G>T
NM_001258274.3:c.-1080G>T	NP_001245203.1:n.-1080G>T
NM_001354615.2:c.-611G>T	NP_001341544.1:n.-611G>T
NM_001354616.2:c.-611G>T	NP_001341545.1:n.-611G>T
NM_001354617.2:c.-703G>T	NP_001341546.1:n.-703G>T
NM_001354618.2:c.-935G>T	NP_001341547.1:n.-935G>T
NM_001354619.2:c.-1059G>T	NP_001341548.1:n.-1059G>T
NM_001354620.2:c.-269G>T	NP_001341549.1:n.-269G>T
NM_001354621.2:c.-1028G>T	NP_001341550.1:n.-1028G>T
NM_001354622.2:c.-1141G>T	NP_001341551.1:n.-1141G>T
NM_001354623.2:c.-1050G>T	NP_001341552.1:n.-1050G>T
NM_001354624.2:c.-811G>T	NP_001341553.1:n.-811G>T
NM_001354625.2:c.-709G>T	NP_001341554.1:n.-709G>T
NM_001354626.2:c.-806G>T	NP_001341555.1:n.-806G>T
NM_001354627.2:c.-1038G>T	NP_001341556.1:n.-1038G>T
NM_001354628.2:c.16G>T	NP_001341557.1:p.Gly6Trp
NM_001354629.2:c.16G>T	NP_001341558.1:p.Gly6Trp
NM_001354630.2:c.16G>T	NP_001341559.1:p.Gly6Trp