Canonical Allele Identifier: CA2702480079

Gene: MLH1

Linked Data

• dbSNP Id: rs2125693018

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.36993523T>G , CM000665.2:g.36993523T>G	GRCh38
NC_000003.11:g.37035014T>G , CM000665.1:g.37035014T>G	GRCh37
NC_000003.10:g.37010018T>G	NCBI36
NG_007109.2:g.5174T>G , LRG_216:g.5174T>G
NG_008418.1:g.4782A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000413740.2:c.-25T>G	ENSP00000416476.2:n.-25T>G
ENST00000450420.6:c.-25T>G	ENSP00000393006.2:n.-25T>G
ENST00000456676.7:c.-25T>G	ENSP00000416687.3:n.-25T>G
ENST00000458009.6:c.-25T>G	ENSP00000411066.2:n.-25T>G
ENST00000616768.6:c.-25T>G	ENSP00000480669.3:n.-25T>G
ENST00000673673.2:c.-25T>G	ENSP00000500979.2:n.-25T>G
ENST00000231790.8:c.-25T>G MANE Select	ENSP00000231790.3:n.-25T>G
ENST00000673713.1:n.7T>G
ENST00000673715.1:c.-25T>G	ENSP00000501301.1:n.-25T>G
ENST00000673899.1:c.-25T>G	ENSP00000501030.1:n.-25T>G
ENST00000673972.1:c.-25T>G	ENSP00000501281.1:n.-25T>G
ENST00000674111.1:c.-25T>G	ENSP00000501162.1:n.-25T>G
ENST00000231790.6:c.-25T>G	ENSP00000231790.2:n.-25T>G
ENST00000457004.5:c.-25T>G	ENSP00000407773.1:n.-25T>G
ENST00000536378.5:c.-657T>G	ENSP00000444286.2:n.-657T>G
NM_000249.3:c.-25T>G , LRG_216t1:c.-25T>G	NP_000240.1:n.-25T>G
NM_001258271.1:c.-25T>G	NP_001245200.1:n.-25T>G
NM_001258273.1:c.-657T>G	NP_001245202.1:n.-657T>G
XM_005265161.1:c.-25T>G	XP_005265218.1:n.-25T>G
XM_005265164.1:c.-743T>G	XP_005265221.1:n.-743T>G
NM_001167617.2:c.-541T>G	NP_001161089.1:n.-541T>G
NM_001167618.2:c.-970T>G	NP_001161090.1:n.-970T>G
NM_001167619.2:c.-883T>G	NP_001161091.1:n.-883T>G
NM_001258274.2:c.-1120T>G	NP_001245203.1:n.-1120T>G
NM_001354615.1:c.-651T>G	NP_001341544.1:n.-651T>G
NM_001354616.1:c.-651T>G	NP_001341545.1:n.-651T>G
NM_001354617.1:c.-743T>G	NP_001341546.1:n.-743T>G
NM_001354618.1:c.-975T>G	NP_001341547.1:n.-975T>G
NM_001354619.1:c.-1099T>G	NP_001341548.1:n.-1099T>G
NM_001354620.1:c.-309T>G	NP_001341549.1:n.-309T>G
NM_001354621.1:c.-1068T>G	NP_001341550.1:n.-1068T>G
NM_001354622.1:c.-1181T>G	NP_001341551.1:n.-1181T>G
NM_001354623.1:c.-1090T>G	NP_001341552.1:n.-1090T>G
NM_001354624.1:c.-851T>G	NP_001341553.1:n.-851T>G
NM_001354625.1:c.-749T>G	NP_001341554.1:n.-749T>G
NM_001354626.1:c.-846T>G	NP_001341555.1:n.-846T>G
NM_001354627.1:c.-1078T>G	NP_001341556.1:n.-1078T>G
NM_001354628.1:c.-25T>G	NP_001341557.1:n.-25T>G
NM_001354629.1:c.-25T>G	NP_001341558.1:n.-25T>G
NM_001354630.1:c.-25T>G	NP_001341559.1:n.-25T>G
XM_005265161.2:c.-25T>G	XP_005265218.1:n.-25T>G
XM_017006450.2:c.-836T>G	XP_016861939.1:n.-836T>G
NM_000249.4:c.-25T>G MANE Select	NP_000240.1:n.-25T>G
NM_001167617.3:c.-541T>G	NP_001161089.1:n.-541T>G
NM_001167618.3:c.-970T>G	NP_001161090.1:n.-970T>G
NM_001167619.3:c.-883T>G	NP_001161091.1:n.-883T>G
NM_001258271.2:c.-25T>G	NP_001245200.1:n.-25T>G
NM_001258273.2:c.-657T>G	NP_001245202.1:n.-657T>G
NM_001258274.3:c.-1120T>G	NP_001245203.1:n.-1120T>G
NM_001354615.2:c.-651T>G	NP_001341544.1:n.-651T>G
NM_001354616.2:c.-651T>G	NP_001341545.1:n.-651T>G
NM_001354617.2:c.-743T>G	NP_001341546.1:n.-743T>G
NM_001354618.2:c.-975T>G	NP_001341547.1:n.-975T>G
NM_001354619.2:c.-1099T>G	NP_001341548.1:n.-1099T>G
NM_001354620.2:c.-309T>G	NP_001341549.1:n.-309T>G
NM_001354621.2:c.-1068T>G	NP_001341550.1:n.-1068T>G
NM_001354622.2:c.-1181T>G	NP_001341551.1:n.-1181T>G
NM_001354623.2:c.-1090T>G	NP_001341552.1:n.-1090T>G
NM_001354624.2:c.-851T>G	NP_001341553.1:n.-851T>G
NM_001354625.2:c.-749T>G	NP_001341554.1:n.-749T>G
NM_001354626.2:c.-846T>G	NP_001341555.1:n.-846T>G
NM_001354627.2:c.-1078T>G	NP_001341556.1:n.-1078T>G
NM_001354628.2:c.-25T>G	NP_001341557.1:n.-25T>G
NM_001354629.2:c.-25T>G	NP_001341558.1:n.-25T>G
NM_001354630.2:c.-25T>G	NP_001341559.1:n.-25T>G