Canonical Allele Identifier: CA007969

Gene: MLH1

Linked Data

• ClinVar Variation Id: 89974
• ClinVar RCV Id: RCV000075456 ; RCV001054272 ; RCV003451090
• dbSNP Id: rs267607879
• MyVariant Identifiers: chr3:g.37090101G>C (hg19) ; chr3:g.37048610G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.37048610G>C , CM000665.2:g.37048610G>C	GRCh38
NC_000003.11:g.37090101G>C , CM000665.1:g.37090101G>C	GRCh37
NC_000003.10:g.37065105G>C	NCBI36
NG_007109.2:g.60261G>C , LRG_216:g.60261G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413740.2:c.1668-1876G>C	ENSP00000416476.2:n.1668-1876G>C
ENST00000429117.6:c.1695+1G>C	ENSP00000407019.2:n.1695+1G>C
ENST00000450420.6:c.1559-1876G>C	ENSP00000393006.2:n.1559-1876G>C
ENST00000456676.7:c.1896+927G>C	ENSP00000416687.3:n.1896+927G>C
ENST00000492474.6:c.1266+1G>C	ENSP00000518393.1:n.1266+1G>C
ENST00000616768.6:c.1897-294G>C	ENSP00000480669.3:n.1897-294G>C
ENST00000673673.2:c.1824+1G>C	ENSP00000500979.2:n.1824+1G>C
ENST00000231790.8:c.1989+1G>C MANE Select	ENSP00000231790.3:n.1989+1G>C
ENST00000413212.2:c.*907+1G>C	ENSP00000400844.2:n.*907+1G>C
ENST00000432299.6:c.*1821+1G>C	ENSP00000416783.1:n.*1821+1G>C
ENST00000447829.6:c.*1100+1G>C	ENSP00000399329.2:n.*1100+1G>C
ENST00000539477.6:c.1266+1G>C	ENSP00000443665.1:n.1266+1G>C
ENST00000616768.5:c.934-294G>C	ENSP00000480669.2:n.934-294G>C
ENST00000673673.1:c.1777+1G>C
ENST00000673741.1:n.1023+1G>C
ENST00000673889.1:n.1371+1G>C
ENST00000673897.1:c.*1781+1G>C	ENSP00000501109.1:n.*1781+1G>C
ENST00000673899.1:c.1257+1G>C	ENSP00000501030.1:n.1257+1G>C
ENST00000673947.1:c.*2129+1G>C	ENSP00000501304.1:n.*2129+1G>C
ENST00000673972.1:c.*1867+1G>C	ENSP00000501281.1:n.*1867+1G>C
ENST00000674019.1:c.1266+1G>C	ENSP00000501081.1:n.1266+1G>C
ENST00000674111.1:c.*218+1G>C	ENSP00000501162.1:n.*218+1G>C
ENST00000674125.1:n.700+1G>C
ENST00000231790.6:c.1989+1G>C	ENSP00000231790.2:n.1989+1G>C
ENST00000413740.1:c.291-1876G>C	ENSP00000416476.1:n.291-1876G>C
ENST00000435176.5:c.1695+1G>C	ENSP00000402564.1:n.1695+1G>C
ENST00000450420.5:c.182-1876G>C	ENSP00000393006.1:n.182-1876G>C
ENST00000455445.6:c.1266+1G>C	ENSP00000398272.2:n.1266+1G>C
ENST00000456676.6:c.1871+927G>C
ENST00000458205.6:c.1266+1G>C	ENSP00000402667.2:n.1266+1G>C
ENST00000536378.5:c.1266+1G>C	ENSP00000444286.2:n.1266+1G>C
ENST00000539477.5:c.1266+1G>C	ENSP00000443665.1:n.1266+1G>C
NM_000249.3:c.1989+1G>C , LRG_216t1:c.1989+1G>C	NP_000240.1:n.1989+1G>C
NM_001167617.1:c.1695+1G>C	NP_001161089.1:n.1695+1G>C
NM_001167618.1:c.1266+1G>C	NP_001161090.1:n.1266+1G>C
NM_001167619.1:c.1266+1G>C	NP_001161091.1:n.1266+1G>C
NM_001258271.1:c.1896+927G>C	NP_001245200.1:n.1896+927G>C
NM_001258273.1:c.1266+1G>C	NP_001245202.1:n.1266+1G>C
NM_001258274.1:c.1266+1G>C	NP_001245203.1:n.1266+1G>C
XM_005265161.1:c.1782+1G>C	XP_005265218.1:n.1782+1G>C
XM_005265163.1:c.1266+1G>C	XP_005265220.1:n.1266+1G>C
XM_005265164.1:c.1266+1G>C	XP_005265221.1:n.1266+1G>C
XM_005265166.1:c.966+1G>C	XP_005265223.1:n.966+1G>C
XM_011533727.1:c.915+1G>C	XP_011532029.1:n.915+1G>C
NM_001167617.2:c.1695+1G>C	NP_001161089.1:n.1695+1G>C
NM_001167618.2:c.1266+1G>C	NP_001161090.1:n.1266+1G>C
NM_001167619.2:c.1266+1G>C	NP_001161091.1:n.1266+1G>C
NM_001258274.2:c.1266+1G>C	NP_001245203.1:n.1266+1G>C
NM_001354615.1:c.1266+1G>C	NP_001341544.1:n.1266+1G>C
NM_001354616.1:c.1266+1G>C	NP_001341545.1:n.1266+1G>C
NM_001354617.1:c.1266+1G>C	NP_001341546.1:n.1266+1G>C
NM_001354618.1:c.1266+1G>C	NP_001341547.1:n.1266+1G>C
NM_001354619.1:c.1266+1G>C	NP_001341548.1:n.1266+1G>C
NM_001354620.1:c.1695+1G>C	NP_001341549.1:n.1695+1G>C
NM_001354621.1:c.966+1G>C	NP_001341550.1:n.966+1G>C
NM_001354622.1:c.966+1G>C	NP_001341551.1:n.966+1G>C
NM_001354623.1:c.966+1G>C	NP_001341552.1:n.966+1G>C
NM_001354624.1:c.915+1G>C	NP_001341553.1:n.915+1G>C
NM_001354625.1:c.915+1G>C	NP_001341554.1:n.915+1G>C
NM_001354626.1:c.915+1G>C	NP_001341555.1:n.915+1G>C
NM_001354627.1:c.915+1G>C	NP_001341556.1:n.915+1G>C
NM_001354628.1:c.1897-294G>C	NP_001341557.1:n.1897-294G>C
NM_001354629.1:c.1890+1G>C	NP_001341558.1:n.1890+1G>C
NM_001354630.1:c.1824+1G>C	NP_001341559.1:n.1824+1G>C
XM_005265161.2:c.1782+1G>C	XP_005265218.1:n.1782+1G>C
XM_017006450.2:c.966+1G>C	XP_016861939.1:n.966+1G>C
NM_000249.4:c.1989+1G>C MANE Select	NP_000240.1:n.1989+1G>C
NM_001167617.3:c.1695+1G>C	NP_001161089.1:n.1695+1G>C
NM_001167618.3:c.1266+1G>C	NP_001161090.1:n.1266+1G>C
NM_001167619.3:c.1266+1G>C	NP_001161091.1:n.1266+1G>C
NM_001258271.2:c.1896+927G>C	NP_001245200.1:n.1896+927G>C
NM_001258273.2:c.1266+1G>C	NP_001245202.1:n.1266+1G>C
NM_001258274.3:c.1266+1G>C	NP_001245203.1:n.1266+1G>C
NM_001354615.2:c.1266+1G>C	NP_001341544.1:n.1266+1G>C
NM_001354616.2:c.1266+1G>C	NP_001341545.1:n.1266+1G>C
NM_001354617.2:c.1266+1G>C	NP_001341546.1:n.1266+1G>C
NM_001354618.2:c.1266+1G>C	NP_001341547.1:n.1266+1G>C
NM_001354619.2:c.1266+1G>C	NP_001341548.1:n.1266+1G>C
NM_001354620.2:c.1695+1G>C	NP_001341549.1:n.1695+1G>C
NM_001354621.2:c.966+1G>C	NP_001341550.1:n.966+1G>C
NM_001354622.2:c.966+1G>C	NP_001341551.1:n.966+1G>C
NM_001354623.2:c.966+1G>C	NP_001341552.1:n.966+1G>C
NM_001354624.2:c.915+1G>C	NP_001341553.1:n.915+1G>C
NM_001354625.2:c.915+1G>C	NP_001341554.1:n.915+1G>C
NM_001354626.2:c.915+1G>C	NP_001341555.1:n.915+1G>C
NM_001354627.2:c.915+1G>C	NP_001341556.1:n.915+1G>C
NM_001354628.2:c.1897-294G>C	NP_001341557.1:n.1897-294G>C
NM_001354629.2:c.1890+1G>C	NP_001341558.1:n.1890+1G>C
NM_001354630.2:c.1824+1G>C	NP_001341559.1:n.1824+1G>C