Canonical Allele Identifier: CA1357880381

Gene: MLH1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.37025825G= , CM000665.2:g.37025825G=	GRCh38
NC_000003.11:g.37067316G= , CM000665.1:g.37067316G=	GRCh37
NC_000003.10:g.37042320G=	NCBI36
NG_007109.2:g.37476G= , LRG_216:g.37476G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413740.2:c.1227G=	ENSP00000416476.2:p.Gln409=
ENST00000429117.6:c.933G=	ENSP00000407019.2:p.Gln311=
ENST00000450420.6:c.1227G=	ENSP00000393006.2:p.Gln409=
ENST00000456676.7:c.1227G=	ENSP00000416687.3:p.Gln409=
ENST00000458009.6:c.*128G=	ENSP00000411066.2:n.*128G=
ENST00000492474.6:c.504G=	ENSP00000518393.1:p.Gln168=
ENST00000616768.6:c.1227G=	ENSP00000480669.3:p.Gln409=
ENST00000673673.2:c.1227G=	ENSP00000500979.2:p.Gln409=
ENST00000231790.8:c.1227G= MANE Select	ENSP00000231790.3:p.Gln409=
ENST00000413212.2:c.*145G=	ENSP00000400844.2:n.*145G=
ENST00000432299.6:c.*1059G=	ENSP00000416783.1:n.*1059G=
ENST00000441265.6:c.504G=	ENSP00000398392.2:p.Gln168=
ENST00000442249.6:n.1035G=
ENST00000447829.6:c.*338G=	ENSP00000399329.2:n.*338G=
ENST00000539477.6:c.504G=	ENSP00000443665.1:p.Gln168=
ENST00000616768.5:c.264G=	ENSP00000480669.2:p.Gln88=
ENST00000673673.1:c.1180G=
ENST00000673713.1:n.1351G=
ENST00000673715.1:c.1227G=	ENSP00000501301.1:p.Gln409=
ENST00000673889.1:n.609G=
ENST00000673897.1:c.*1019G=	ENSP00000501109.1:n.*1019G=
ENST00000673899.1:c.678-2959G=	ENSP00000501030.1:n.678-2959G=
ENST00000673947.1:c.*1367G=	ENSP00000501304.1:n.*1367G=
ENST00000673972.1:c.*1105G=	ENSP00000501281.1:n.*1105G=
ENST00000673990.1:n.1118G=
ENST00000674019.1:c.504G=	ENSP00000501081.1:p.Gln168=
ENST00000674107.1:n.1075G=
ENST00000674111.1:c.1227G=	ENSP00000501162.1:p.Gln409=
ENST00000231790.6:c.1227G=	ENSP00000231790.2:p.Gln409=
ENST00000413212.1:c.302G=
ENST00000435176.5:c.933G=	ENSP00000402564.1:p.Gln311=
ENST00000447829.5:c.514G=
ENST00000455445.6:c.504G=	ENSP00000398272.2:p.Gln168=
ENST00000456676.6:c.1202G=
ENST00000458009.5:c.414G=
ENST00000458205.6:c.504G=	ENSP00000402667.2:p.Gln168=
ENST00000536378.5:c.504G=	ENSP00000444286.2:p.Gln168=
ENST00000539477.5:c.504G=	ENSP00000443665.1:p.Gln168=
NM_000249.3:c.1227G= , LRG_216t1:c.1227G=	NP_000240.1:p.Gln409=
NM_001167617.1:c.933G=	NP_001161089.1:p.Gln311=
NM_001167618.1:c.504G=	NP_001161090.1:p.Gln168=
NM_001167619.1:c.504G=	NP_001161091.1:p.Gln168=
NM_001258271.1:c.1227G=	NP_001245200.1:p.Gln409=
NM_001258273.1:c.504G=	NP_001245202.1:p.Gln168=
NM_001258274.1:c.504G=	NP_001245203.1:p.Gln168=
XM_005265161.1:c.1020G=	XP_005265218.1:p.Gln340=
XM_005265163.1:c.504G=	XP_005265220.1:p.Gln168=
XM_005265164.1:c.504G=	XP_005265221.1:p.Gln168=
XM_005265166.1:c.204G=	XP_005265223.1:p.Gln68=
XM_011533727.1:c.153G=	XP_011532029.1:p.Gln51=
NM_001167617.2:c.933G=	NP_001161089.1:p.Gln311=
NM_001167618.2:c.504G=	NP_001161090.1:p.Gln168=
NM_001167619.2:c.504G=	NP_001161091.1:p.Gln168=
NM_001258274.2:c.504G=	NP_001245203.1:p.Gln168=
NM_001354615.1:c.504G=	NP_001341544.1:p.Gln168=
NM_001354616.1:c.504G=	NP_001341545.1:p.Gln168=
NM_001354617.1:c.504G=	NP_001341546.1:p.Gln168=
NM_001354618.1:c.504G=	NP_001341547.1:p.Gln168=
NM_001354619.1:c.504G=	NP_001341548.1:p.Gln168=
NM_001354620.1:c.933G=	NP_001341549.1:p.Gln311=
NM_001354621.1:c.204G=	NP_001341550.1:p.Gln68=
NM_001354622.1:c.204G=	NP_001341551.1:p.Gln68=
NM_001354623.1:c.204G=	NP_001341552.1:p.Gln68=
NM_001354624.1:c.153G=	NP_001341553.1:p.Gln51=
NM_001354625.1:c.153G=	NP_001341554.1:p.Gln51=
NM_001354626.1:c.153G=	NP_001341555.1:p.Gln51=
NM_001354627.1:c.153G=	NP_001341556.1:p.Gln51=
NM_001354628.1:c.1227G=	NP_001341557.1:p.Gln409=
NM_001354629.1:c.1128G=	NP_001341558.1:p.Gln376=
NM_001354630.1:c.1227G=	NP_001341559.1:p.Gln409=
XM_005265161.2:c.1020G=	XP_005265218.1:p.Gln340=
XM_017006450.2:c.204G=	XP_016861939.1:p.Gln68=
NM_000249.4:c.1227G= MANE Select	NP_000240.1:p.Gln409=
NM_001167617.3:c.933G=	NP_001161089.1:p.Gln311=
NM_001167618.3:c.504G=	NP_001161090.1:p.Gln168=
NM_001167619.3:c.504G=	NP_001161091.1:p.Gln168=
NM_001258271.2:c.1227G=	NP_001245200.1:p.Gln409=
NM_001258273.2:c.504G=	NP_001245202.1:p.Gln168=
NM_001258274.3:c.504G=	NP_001245203.1:p.Gln168=
NM_001354615.2:c.504G=	NP_001341544.1:p.Gln168=
NM_001354616.2:c.504G=	NP_001341545.1:p.Gln168=
NM_001354617.2:c.504G=	NP_001341546.1:p.Gln168=
NM_001354618.2:c.504G=	NP_001341547.1:p.Gln168=
NM_001354619.2:c.504G=	NP_001341548.1:p.Gln168=
NM_001354620.2:c.933G=	NP_001341549.1:p.Gln311=
NM_001354621.2:c.204G=	NP_001341550.1:p.Gln68=
NM_001354622.2:c.204G=	NP_001341551.1:p.Gln68=
NM_001354623.2:c.204G=	NP_001341552.1:p.Gln68=
NM_001354624.2:c.153G=	NP_001341553.1:p.Gln51=
NM_001354625.2:c.153G=	NP_001341554.1:p.Gln51=
NM_001354626.2:c.153G=	NP_001341555.1:p.Gln51=
NM_001354627.2:c.153G=	NP_001341556.1:p.Gln51=
NM_001354628.2:c.1227G=	NP_001341557.1:p.Gln409=
NM_001354629.2:c.1128G=	NP_001341558.1:p.Gln376=
NM_001354630.2:c.1227G=	NP_001341559.1:p.Gln409=