Canonical Allele Identifier: CA1357864899

Gene: MLH1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.36993649G= , CM000665.2:g.36993649G=	GRCh38
NC_000003.11:g.37035140G= , CM000665.1:g.37035140G=	GRCh37
NC_000003.10:g.37010144G=	NCBI36
NG_007109.2:g.5300G= , LRG_216:g.5300G=
NG_008418.1:g.4656C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413740.2:c.102G=	ENSP00000416476.2:p.Glu34=
ENST00000450420.6:c.102G=	ENSP00000393006.2:p.Glu34=
ENST00000456676.7:c.102G=	ENSP00000416687.3:p.Glu34=
ENST00000458009.6:c.102G=	ENSP00000411066.2:p.Glu34=
ENST00000616768.6:c.102G=	ENSP00000480669.3:p.Glu34=
ENST00000673673.2:c.102G=	ENSP00000500979.2:p.Glu34=
ENST00000231790.8:c.102G= MANE Select	ENSP00000231790.3:p.Glu34=
ENST00000432299.6:c.102G=	ENSP00000416783.1:p.Glu34=
ENST00000442249.6:n.117G=
ENST00000673673.1:c.55G=
ENST00000673713.1:n.133G=
ENST00000673715.1:c.102G=	ENSP00000501301.1:p.Glu34=
ENST00000673897.1:c.102G=	ENSP00000501109.1:p.Glu34=
ENST00000673899.1:c.102G=	ENSP00000501030.1:p.Glu34=
ENST00000673947.1:c.102G=	ENSP00000501304.1:p.Glu34=
ENST00000673972.1:c.102G=	ENSP00000501281.1:p.Glu34=
ENST00000674111.1:c.102G=	ENSP00000501162.1:p.Glu34=
ENST00000231790.6:c.102G=	ENSP00000231790.2:p.Glu34=
ENST00000432299.5:c.102G=	ENSP00000416783.1:p.Glu34=
ENST00000442249.5:c.102G=	ENSP00000387511.1:p.Glu34=
ENST00000454028.5:c.102G=	ENSP00000392649.1:p.Glu34=
ENST00000456676.6:c.77G=
ENST00000457004.5:c.102G=	ENSP00000407773.1:p.Glu34=
ENST00000536378.5:c.-531G=	ENSP00000444286.2:n.-531G=
NM_000249.3:c.102G= , LRG_216t1:c.102G=	NP_000240.1:p.Glu34=
NM_001258271.1:c.102G=	NP_001245200.1:p.Glu34=
NM_001258273.1:c.-531G=	NP_001245202.1:n.-531G=
XM_005265161.1:c.102G=	XP_005265218.1:p.Glu34=
XM_005265164.1:c.-617G=	XP_005265221.1:n.-617G=
NM_001167617.2:c.-415G=	NP_001161089.1:n.-415G=
NM_001167618.2:c.-844G=	NP_001161090.1:n.-844G=
NM_001167619.2:c.-757G=	NP_001161091.1:n.-757G=
NM_001258274.2:c.-994G=	NP_001245203.1:n.-994G=
NM_001354615.1:c.-525G=	NP_001341544.1:n.-525G=
NM_001354616.1:c.-525G=	NP_001341545.1:n.-525G=
NM_001354617.1:c.-617G=	NP_001341546.1:n.-617G=
NM_001354618.1:c.-849G=	NP_001341547.1:n.-849G=
NM_001354619.1:c.-973G=	NP_001341548.1:n.-973G=
NM_001354620.1:c.-183G=	NP_001341549.1:n.-183G=
NM_001354621.1:c.-942G=	NP_001341550.1:n.-942G=
NM_001354622.1:c.-1055G=	NP_001341551.1:n.-1055G=
NM_001354623.1:c.-964G=	NP_001341552.1:n.-964G=
NM_001354624.1:c.-725G=	NP_001341553.1:n.-725G=
NM_001354625.1:c.-623G=	NP_001341554.1:n.-623G=
NM_001354626.1:c.-720G=	NP_001341555.1:n.-720G=
NM_001354627.1:c.-952G=	NP_001341556.1:n.-952G=
NM_001354628.1:c.102G=	NP_001341557.1:p.Glu34=
NM_001354629.1:c.102G=	NP_001341558.1:p.Glu34=
NM_001354630.1:c.102G=	NP_001341559.1:p.Glu34=
XM_005265161.2:c.102G=	XP_005265218.1:p.Glu34=
XM_017006450.2:c.-710G=	XP_016861939.1:n.-710G=
NM_000249.4:c.102G= MANE Select	NP_000240.1:p.Glu34=
NM_001167617.3:c.-415G=	NP_001161089.1:n.-415G=
NM_001167618.3:c.-844G=	NP_001161090.1:n.-844G=
NM_001167619.3:c.-757G=	NP_001161091.1:n.-757G=
NM_001258271.2:c.102G=	NP_001245200.1:p.Glu34=
NM_001258273.2:c.-531G=	NP_001245202.1:n.-531G=
NM_001258274.3:c.-994G=	NP_001245203.1:n.-994G=
NM_001354615.2:c.-525G=	NP_001341544.1:n.-525G=
NM_001354616.2:c.-525G=	NP_001341545.1:n.-525G=
NM_001354617.2:c.-617G=	NP_001341546.1:n.-617G=
NM_001354618.2:c.-849G=	NP_001341547.1:n.-849G=
NM_001354619.2:c.-973G=	NP_001341548.1:n.-973G=
NM_001354620.2:c.-183G=	NP_001341549.1:n.-183G=
NM_001354621.2:c.-942G=	NP_001341550.1:n.-942G=
NM_001354622.2:c.-1055G=	NP_001341551.1:n.-1055G=
NM_001354623.2:c.-964G=	NP_001341552.1:n.-964G=
NM_001354624.2:c.-725G=	NP_001341553.1:n.-725G=
NM_001354625.2:c.-623G=	NP_001341554.1:n.-623G=
NM_001354626.2:c.-720G=	NP_001341555.1:n.-720G=
NM_001354627.2:c.-952G=	NP_001341556.1:n.-952G=
NM_001354628.2:c.102G=	NP_001341557.1:p.Glu34=
NM_001354629.2:c.102G=	NP_001341558.1:p.Glu34=
NM_001354630.2:c.102G=	NP_001341559.1:p.Glu34=