Canonical Allele Identifier: CA012277

Gene: MLH1

Linked Data

• ClinVar Variation Id: 90369
• ClinVar RCV Id: RCV000075860 ; RCV001183311 ; RCV001388082 ; RCV002247470 ; RCV001723644 ; RCV003452771
• dbSNP Id: rs267607795
• MyVariant Identifiers: chr3:g.37058996G>C (hg19) ; chr3:g.37017505G>C (hg38)
• PubMed: PMID:8571956 ; PMID:9311737 ; PMID:12414824

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.37017505G>C , CM000665.2:g.37017505G>C	GRCh38
NC_000003.11:g.37058996G>C , CM000665.1:g.37058996G>C	GRCh37
NC_000003.10:g.37034000G>C	NCBI36
NG_007109.2:g.29156G>C , LRG_216:g.29156G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413740.2:c.791-1G>C	ENSP00000416476.2:n.791-1G>C
ENST00000429117.6:c.497-1G>C	ENSP00000407019.2:n.497-1G>C
ENST00000450420.6:c.791-1G>C	ENSP00000393006.2:n.791-1G>C
ENST00000456676.7:c.791-1G>C	ENSP00000416687.3:n.791-1G>C
ENST00000458009.6:c.791-1G>C	ENSP00000411066.2:n.791-1G>C
ENST00000492474.6:c.68-1G>C	ENSP00000518393.1:n.68-1G>C
ENST00000616768.6:c.791-1G>C	ENSP00000480669.3:n.791-1G>C
ENST00000673673.2:c.791-1G>C	ENSP00000500979.2:n.791-1G>C
ENST00000231790.8:c.791-1G>C MANE Select	ENSP00000231790.3:n.791-1G>C
ENST00000413212.2:c.67+2961G>C	ENSP00000400844.2:n.67+2961G>C
ENST00000432299.6:c.*870+2961G>C	ENSP00000416783.1:n.*870+2961G>C
ENST00000441265.6:c.68-1G>C	ENSP00000398392.2:n.68-1G>C
ENST00000442249.6:n.693-2805G>C
ENST00000447829.6:c.428-2805G>C	ENSP00000399329.2:n.428-2805G>C
ENST00000539477.6:c.68-1G>C	ENSP00000443665.1:n.68-1G>C
ENST00000673673.1:c.744-1G>C
ENST00000673713.1:n.822-1G>C
ENST00000673715.1:c.791-1G>C	ENSP00000501301.1:n.791-1G>C
ENST00000673889.1:n.172G>C
ENST00000673897.1:c.*583-1G>C	ENSP00000501109.1:n.*583-1G>C
ENST00000673899.1:c.677+5406G>C	ENSP00000501030.1:n.677+5406G>C
ENST00000673947.1:c.*931-1G>C	ENSP00000501304.1:n.*931-1G>C
ENST00000673972.1:c.*669-1G>C	ENSP00000501281.1:n.*669-1G>C
ENST00000673990.1:n.776-2805G>C
ENST00000674019.1:c.68-1G>C	ENSP00000501081.1:n.68-1G>C
ENST00000674107.1:n.733-2805G>C
ENST00000674111.1:c.791-1G>C	ENSP00000501162.1:n.791-1G>C
ENST00000231790.6:c.791-1G>C	ENSP00000231790.2:n.791-1G>C
ENST00000413212.1:c.113+2961G>C
ENST00000435176.5:c.497-1G>C	ENSP00000402564.1:n.497-1G>C
ENST00000441265.5:c.68-1G>C	ENSP00000398392.1:n.68-1G>C
ENST00000447829.5:c.172-2805G>C
ENST00000455445.6:c.68-1G>C	ENSP00000398272.2:n.68-1G>C
ENST00000456676.6:c.766-1G>C
ENST00000458009.5:c.132-1G>C
ENST00000458205.6:c.68-1G>C	ENSP00000402667.2:n.68-1G>C
ENST00000536378.5:c.68-1G>C	ENSP00000444286.2:n.68-1G>C
ENST00000539477.5:c.68-1G>C	ENSP00000443665.1:n.68-1G>C
NM_000249.3:c.791-1G>C , LRG_216t1:c.791-1G>C	NP_000240.1:n.791-1G>C
NM_001167617.1:c.497-1G>C	NP_001161089.1:n.497-1G>C
NM_001167618.1:c.68-1G>C	NP_001161090.1:n.68-1G>C
NM_001167619.1:c.68-1G>C	NP_001161091.1:n.68-1G>C
NM_001258271.1:c.791-1G>C	NP_001245200.1:n.791-1G>C
NM_001258273.1:c.68-1G>C	NP_001245202.1:n.68-1G>C
NM_001258274.1:c.68-1G>C	NP_001245203.1:n.68-1G>C
XM_005265161.1:c.678-2805G>C	XP_005265218.1:n.678-2805G>C
XM_005265163.1:c.68-1G>C	XP_005265220.1:n.68-1G>C
XM_005265164.1:c.68-1G>C	XP_005265221.1:n.68-1G>C
XM_005265166.1:c.-139-2805G>C	XP_005265223.1:n.-139-2805G>C
XM_011533727.1:c.-37+2961G>C	XP_011532029.1:n.-37+2961G>C
NM_001167617.2:c.497-1G>C	NP_001161089.1:n.497-1G>C
NM_001167618.2:c.68-1G>C	NP_001161090.1:n.68-1G>C
NM_001167619.2:c.68-1G>C	NP_001161091.1:n.68-1G>C
NM_001258274.2:c.68-1G>C	NP_001245203.1:n.68-1G>C
NM_001354615.1:c.68-1G>C	NP_001341544.1:n.68-1G>C
NM_001354616.1:c.68-1G>C	NP_001341545.1:n.68-1G>C
NM_001354617.1:c.68-1G>C	NP_001341546.1:n.68-1G>C
NM_001354618.1:c.68-1G>C	NP_001341547.1:n.68-1G>C
NM_001354619.1:c.68-1G>C	NP_001341548.1:n.68-1G>C
NM_001354620.1:c.497-1G>C	NP_001341549.1:n.497-1G>C
NM_001354621.1:c.-139-2805G>C	NP_001341550.1:n.-139-2805G>C
NM_001354622.1:c.-139-2805G>C	NP_001341551.1:n.-139-2805G>C
NM_001354623.1:c.-139-2805G>C	NP_001341552.1:n.-139-2805G>C
NM_001354624.1:c.-37+2961G>C	NP_001341553.1:n.-37+2961G>C
NM_001354625.1:c.-37+2961G>C	NP_001341554.1:n.-37+2961G>C
NM_001354626.1:c.-37+2961G>C	NP_001341555.1:n.-37+2961G>C
NM_001354627.1:c.-37+2961G>C	NP_001341556.1:n.-37+2961G>C
NM_001354628.1:c.791-1G>C	NP_001341557.1:n.791-1G>C
NM_001354629.1:c.692-1G>C	NP_001341558.1:n.692-1G>C
NM_001354630.1:c.791-1G>C	NP_001341559.1:n.791-1G>C
XM_005265161.2:c.678-2805G>C	XP_005265218.1:n.678-2805G>C
XM_017006450.2:c.-139-2805G>C	XP_016861939.1:n.-139-2805G>C
NM_000249.4:c.791-1G>C MANE Select	NP_000240.1:n.791-1G>C
NM_001167617.3:c.497-1G>C	NP_001161089.1:n.497-1G>C
NM_001167618.3:c.68-1G>C	NP_001161090.1:n.68-1G>C
NM_001167619.3:c.68-1G>C	NP_001161091.1:n.68-1G>C
NM_001258271.2:c.791-1G>C	NP_001245200.1:n.791-1G>C
NM_001258273.2:c.68-1G>C	NP_001245202.1:n.68-1G>C
NM_001258274.3:c.68-1G>C	NP_001245203.1:n.68-1G>C
NM_001354615.2:c.68-1G>C	NP_001341544.1:n.68-1G>C
NM_001354616.2:c.68-1G>C	NP_001341545.1:n.68-1G>C
NM_001354617.2:c.68-1G>C	NP_001341546.1:n.68-1G>C
NM_001354618.2:c.68-1G>C	NP_001341547.1:n.68-1G>C
NM_001354619.2:c.68-1G>C	NP_001341548.1:n.68-1G>C
NM_001354620.2:c.497-1G>C	NP_001341549.1:n.497-1G>C
NM_001354621.2:c.-139-2805G>C	NP_001341550.1:n.-139-2805G>C
NM_001354622.2:c.-139-2805G>C	NP_001341551.1:n.-139-2805G>C
NM_001354623.2:c.-139-2805G>C	NP_001341552.1:n.-139-2805G>C
NM_001354624.2:c.-37+2961G>C	NP_001341553.1:n.-37+2961G>C
NM_001354625.2:c.-37+2961G>C	NP_001341554.1:n.-37+2961G>C
NM_001354626.2:c.-37+2961G>C	NP_001341555.1:n.-37+2961G>C
NM_001354627.2:c.-37+2961G>C	NP_001341556.1:n.-37+2961G>C
NM_001354628.2:c.791-1G>C	NP_001341557.1:n.791-1G>C
NM_001354629.2:c.692-1G>C	NP_001341558.1:n.692-1G>C
NM_001354630.2:c.791-1G>C	NP_001341559.1:n.791-1G>C