Canonical Allele Identifier: CA352041060

Gene: MLH1

Linked Data

• ClinVar Variation Id: 525800
• ClinVar RCV Id: RCV000630108 ; RCV001023939 ; RCV003465387
• dbSNP Id: rs1248251121
• gnomAD v4: 3-37008892-G-A
• MyVariant Identifiers: chr3:g.37050383G>A (hg19) ; chr3:g.37008892G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.37008892G>A , CM000665.2:g.37008892G>A	GRCh38
NC_000003.11:g.37050383G>A , CM000665.1:g.37050383G>A	GRCh37
NC_000003.10:g.37025387G>A	NCBI36
NG_007109.2:g.20543G>A , LRG_216:g.20543G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413740.2:c.532G>A	ENSP00000416476.2:p.Glu178Lys
ENST00000429117.6:c.238G>A	ENSP00000407019.2:p.Glu80Lys
ENST00000450420.6:c.532G>A	ENSP00000393006.2:p.Glu178Lys
ENST00000456676.7:c.532G>A	ENSP00000416687.3:p.Glu178Lys
ENST00000458009.6:c.532G>A	ENSP00000411066.2:p.Glu178Lys
ENST00000492474.6:c.-192G>A	ENSP00000518393.1:n.-192G>A
ENST00000616768.6:c.532G>A	ENSP00000480669.3:p.Glu178Lys
ENST00000673673.2:c.532G>A	ENSP00000500979.2:p.Glu178Lys
ENST00000231790.8:c.532G>A MANE Select	ENSP00000231790.3:p.Glu178Lys
ENST00000413212.2:c.-192G>A	ENSP00000400844.2:n.-192G>A
ENST00000432299.6:c.*612G>A	ENSP00000416783.1:n.*612G>A
ENST00000441265.6:c.-192G>A	ENSP00000398392.2:n.-192G>A
ENST00000442249.6:n.547G>A
ENST00000447829.6:c.169G>A	ENSP00000399329.2:p.Glu57Lys
ENST00000539477.6:c.-179+1829G>A	ENSP00000443665.1:n.-179+1829G>A
ENST00000673673.1:c.485G>A
ENST00000673713.1:n.563G>A
ENST00000673715.1:c.532G>A	ENSP00000501301.1:p.Glu178Lys
ENST00000673897.1:c.*324G>A	ENSP00000501109.1:n.*324G>A
ENST00000673899.1:c.532G>A	ENSP00000501030.1:p.Glu178Lys
ENST00000673947.1:c.*672G>A	ENSP00000501304.1:n.*672G>A
ENST00000673972.1:c.*410G>A	ENSP00000501281.1:n.*410G>A
ENST00000673990.1:n.517G>A
ENST00000674019.1:c.-192G>A	ENSP00000501081.1:n.-192G>A
ENST00000674107.1:n.474G>A
ENST00000674111.1:c.532G>A	ENSP00000501162.1:p.Glu178Lys
ENST00000231790.6:c.532G>A	ENSP00000231790.2:p.Glu178Lys
ENST00000429117.5:c.238G>A	ENSP00000407019.1:p.Glu80Lys
ENST00000432299.5:c.*612G>A	ENSP00000416783.1:n.*612G>A
ENST00000435176.5:c.238G>A	ENSP00000402564.1:p.Glu80Lys
ENST00000441265.5:c.-179+1829G>A	ENSP00000398392.1:n.-179+1829G>A
ENST00000442249.5:c.*324G>A	ENSP00000387511.1:n.*324G>A
ENST00000454028.5:c.*405G>A	ENSP00000392649.1:n.*405G>A
ENST00000455445.6:c.-192G>A	ENSP00000398272.2:n.-192G>A
ENST00000456676.6:c.507G>A
ENST00000457004.5:c.*311G>A	ENSP00000407773.1:n.*311G>A
ENST00000458205.6:c.-192G>A	ENSP00000402667.2:n.-192G>A
ENST00000485889.1:n.536G>A
ENST00000492474.5:n.555G>A
ENST00000536378.5:c.-192G>A	ENSP00000444286.2:n.-192G>A
ENST00000539477.5:c.-179+1829G>A	ENSP00000443665.1:n.-179+1829G>A
NM_000249.3:c.532G>A , LRG_216t1:c.532G>A	NP_000240.1:p.Glu178Lys
NM_001167617.1:c.238G>A	NP_001161089.1:p.Glu80Lys
NM_001167618.1:c.-192G>A	NP_001161090.1:n.-192G>A
NM_001167619.1:c.-179+1829G>A	NP_001161091.1:n.-179+1829G>A
NM_001258271.1:c.532G>A	NP_001245200.1:p.Glu178Lys
NM_001258273.1:c.-192G>A	NP_001245202.1:n.-192G>A
NM_001258274.1:c.-192G>A	NP_001245203.1:n.-192G>A
XM_005265161.1:c.532G>A	XP_005265218.1:p.Glu178Lys
XM_005265163.1:c.-192G>A	XP_005265220.1:n.-192G>A
XM_005265164.1:c.-192G>A	XP_005265221.1:n.-192G>A
XM_005265166.1:c.-398G>A	XP_005265223.1:n.-398G>A
XM_011533727.1:c.-295G>A	XP_011532029.1:n.-295G>A
NM_001167617.2:c.238G>A	NP_001161089.1:p.Glu80Lys
NM_001167618.2:c.-192G>A	NP_001161090.1:n.-192G>A
NM_001167619.2:c.-179+1829G>A	NP_001161091.1:n.-179+1829G>A
NM_001258274.2:c.-192G>A	NP_001245203.1:n.-192G>A
NM_001354615.1:c.-179+1829G>A	NP_001341544.1:n.-179+1829G>A
NM_001354616.1:c.-179+1829G>A	NP_001341545.1:n.-179+1829G>A
NM_001354617.1:c.-192G>A	NP_001341546.1:n.-192G>A
NM_001354618.1:c.-192G>A	NP_001341547.1:n.-192G>A
NM_001354619.1:c.-192G>A	NP_001341548.1:n.-192G>A
NM_001354620.1:c.238G>A	NP_001341549.1:p.Glu80Lys
NM_001354621.1:c.-285G>A	NP_001341550.1:n.-285G>A
NM_001354622.1:c.-398G>A	NP_001341551.1:n.-398G>A
NM_001354623.1:c.-398G>A	NP_001341552.1:n.-398G>A
NM_001354624.1:c.-295G>A	NP_001341553.1:n.-295G>A
NM_001354625.1:c.-282+1829G>A	NP_001341554.1:n.-282+1829G>A
NM_001354626.1:c.-295G>A	NP_001341555.1:n.-295G>A
NM_001354627.1:c.-295G>A	NP_001341556.1:n.-295G>A
NM_001354628.1:c.532G>A	NP_001341557.1:p.Glu178Lys
NM_001354629.1:c.433G>A	NP_001341558.1:p.Glu145Lys
NM_001354630.1:c.532G>A	NP_001341559.1:p.Glu178Lys
XM_005265161.2:c.532G>A	XP_005265218.1:p.Glu178Lys
XM_017006450.2:c.-285G>A	XP_016861939.1:n.-285G>A
NM_000249.4:c.532G>A MANE Select	NP_000240.1:p.Glu178Lys
NM_001167617.3:c.238G>A	NP_001161089.1:p.Glu80Lys
NM_001167618.3:c.-192G>A	NP_001161090.1:n.-192G>A
NM_001167619.3:c.-179+1829G>A	NP_001161091.1:n.-179+1829G>A
NM_001258271.2:c.532G>A	NP_001245200.1:p.Glu178Lys
NM_001258273.2:c.-192G>A	NP_001245202.1:n.-192G>A
NM_001258274.3:c.-192G>A	NP_001245203.1:n.-192G>A
NM_001354615.2:c.-179+1829G>A	NP_001341544.1:n.-179+1829G>A
NM_001354616.2:c.-179+1829G>A	NP_001341545.1:n.-179+1829G>A
NM_001354617.2:c.-192G>A	NP_001341546.1:n.-192G>A
NM_001354618.2:c.-192G>A	NP_001341547.1:n.-192G>A
NM_001354619.2:c.-192G>A	NP_001341548.1:n.-192G>A
NM_001354620.2:c.238G>A	NP_001341549.1:p.Glu80Lys
NM_001354621.2:c.-285G>A	NP_001341550.1:n.-285G>A
NM_001354622.2:c.-398G>A	NP_001341551.1:n.-398G>A
NM_001354623.2:c.-398G>A	NP_001341552.1:n.-398G>A
NM_001354624.2:c.-295G>A	NP_001341553.1:n.-295G>A
NM_001354625.2:c.-282+1829G>A	NP_001341554.1:n.-282+1829G>A
NM_001354626.2:c.-295G>A	NP_001341555.1:n.-295G>A
NM_001354627.2:c.-295G>A	NP_001341556.1:n.-295G>A
NM_001354628.2:c.532G>A	NP_001341557.1:p.Glu178Lys
NM_001354629.2:c.433G>A	NP_001341558.1:p.Glu145Lys
NM_001354630.2:c.532G>A	NP_001341559.1:p.Glu178Lys