Canonical Allele Identifier: CA433086940

Gene: MLH1

Linked Data

• MyVariant Identifiers: chr3:g.37092066T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.37050575T>G , CM000665.2:g.37050575T>G	GRCh38
NC_000003.11:g.37092066T>G , CM000665.1:g.37092066T>G	GRCh37
NC_000003.10:g.37067070T>G	NCBI36
NG_007109.2:g.62226T>G , LRG_216:g.62226T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413740.2:c.1757T>G	ENSP00000416476.2:p.Leu586Arg
ENST00000429117.6:c.1899T>G	ENSP00000407019.2:p.Pro633=
ENST00000456676.7:c.1986T>G	ENSP00000416687.3:p.Pro662=
ENST00000492474.6:c.1470T>G	ENSP00000518393.1:p.Pro490=
ENST00000616768.6:c.2100T>G	ENSP00000480669.3:p.Pro700=
ENST00000673673.2:c.2028T>G	ENSP00000500979.2:p.Pro676=
ENST00000231790.8:c.2193T>G MANE Select	ENSP00000231790.3:p.Pro731=
ENST00000413212.2:c.*1111T>G	ENSP00000400844.2:n.*1111T>G
ENST00000432299.6:c.*2025T>G	ENSP00000416783.1:n.*2025T>G
ENST00000447829.6:c.*1304T>G	ENSP00000399329.2:n.*1304T>G
ENST00000539477.6:c.1470T>G	ENSP00000443665.1:p.Pro490=
ENST00000616768.5:c.1137T>G	ENSP00000480669.2:p.Pro379=
ENST00000673673.1:c.1981T>G
ENST00000673741.1:n.1227T>G
ENST00000673889.1:n.1575T>G
ENST00000673897.1:c.*1985T>G	ENSP00000501109.1:n.*1985T>G
ENST00000673899.1:c.1461T>G	ENSP00000501030.1:p.Pro487=
ENST00000673947.1:c.*2333T>G	ENSP00000501304.1:n.*2333T>G
ENST00000673972.1:c.*2071T>G	ENSP00000501281.1:n.*2071T>G
ENST00000674019.1:c.1470T>G	ENSP00000501081.1:p.Pro490=
ENST00000674111.1:c.*422T>G	ENSP00000501162.1:n.*422T>G
ENST00000674125.1:n.904T>G
ENST00000231790.6:c.2193T>G	ENSP00000231790.2:p.Pro731=
ENST00000435176.5:c.1899T>G	ENSP00000402564.1:p.Pro633=
ENST00000455445.6:c.1470T>G	ENSP00000398272.2:p.Pro490=
ENST00000456676.6:c.1961T>G
ENST00000458205.6:c.1470T>G	ENSP00000402667.2:p.Pro490=
ENST00000536378.5:c.1470T>G	ENSP00000444286.2:p.Pro490=
ENST00000539477.5:c.1470T>G	ENSP00000443665.1:p.Pro490=
NM_000249.3:c.2193T>G , LRG_216t1:c.2193T>G	NP_000240.1:p.Pro731=
NM_001167617.1:c.1899T>G	NP_001161089.1:p.Pro633=
NM_001167618.1:c.1470T>G	NP_001161090.1:p.Pro490=
NM_001167619.1:c.1470T>G	NP_001161091.1:p.Pro490=
NM_001258271.1:c.1986T>G	NP_001245200.1:p.Pro662=
NM_001258273.1:c.1470T>G	NP_001245202.1:p.Pro490=
NM_001258274.1:c.1470T>G	NP_001245203.1:p.Pro490=
XM_005265161.1:c.1986T>G	XP_005265218.1:p.Pro662=
XM_005265163.1:c.1470T>G	XP_005265220.1:p.Pro490=
XM_005265164.1:c.1470T>G	XP_005265221.1:p.Pro490=
XM_005265166.1:c.1170T>G	XP_005265223.1:p.Pro390=
XM_011533727.1:c.1119T>G	XP_011532029.1:p.Pro373=
NM_001167617.2:c.1899T>G	NP_001161089.1:p.Pro633=
NM_001167618.2:c.1470T>G	NP_001161090.1:p.Pro490=
NM_001167619.2:c.1470T>G	NP_001161091.1:p.Pro490=
NM_001258274.2:c.1470T>G	NP_001245203.1:p.Pro490=
NM_001354615.1:c.1470T>G	NP_001341544.1:p.Pro490=
NM_001354616.1:c.1470T>G	NP_001341545.1:p.Pro490=
NM_001354617.1:c.1470T>G	NP_001341546.1:p.Pro490=
NM_001354618.1:c.1470T>G	NP_001341547.1:p.Pro490=
NM_001354619.1:c.1470T>G	NP_001341548.1:p.Pro490=
NM_001354620.1:c.1899T>G	NP_001341549.1:p.Pro633=
NM_001354621.1:c.1170T>G	NP_001341550.1:p.Pro390=
NM_001354622.1:c.1170T>G	NP_001341551.1:p.Pro390=
NM_001354623.1:c.1170T>G	NP_001341552.1:p.Pro390=
NM_001354624.1:c.1119T>G	NP_001341553.1:p.Pro373=
NM_001354625.1:c.1119T>G	NP_001341554.1:p.Pro373=
NM_001354626.1:c.1119T>G	NP_001341555.1:p.Pro373=
NM_001354627.1:c.1119T>G	NP_001341556.1:p.Pro373=
NM_001354628.1:c.2100T>G	NP_001341557.1:p.Pro700=
NM_001354629.1:c.2094T>G	NP_001341558.1:p.Pro698=
NM_001354630.1:c.2028T>G	NP_001341559.1:p.Pro676=
XM_005265161.2:c.1986T>G	XP_005265218.1:p.Pro662=
XM_017006450.2:c.1170T>G	XP_016861939.1:p.Pro390=
NM_000249.4:c.2193T>G MANE Select	NP_000240.1:p.Pro731=
NM_001167617.3:c.1899T>G	NP_001161089.1:p.Pro633=
NM_001167618.3:c.1470T>G	NP_001161090.1:p.Pro490=
NM_001167619.3:c.1470T>G	NP_001161091.1:p.Pro490=
NM_001258271.2:c.1986T>G	NP_001245200.1:p.Pro662=
NM_001258273.2:c.1470T>G	NP_001245202.1:p.Pro490=
NM_001258274.3:c.1470T>G	NP_001245203.1:p.Pro490=
NM_001354615.2:c.1470T>G	NP_001341544.1:p.Pro490=
NM_001354616.2:c.1470T>G	NP_001341545.1:p.Pro490=
NM_001354617.2:c.1470T>G	NP_001341546.1:p.Pro490=
NM_001354618.2:c.1470T>G	NP_001341547.1:p.Pro490=
NM_001354619.2:c.1470T>G	NP_001341548.1:p.Pro490=
NM_001354620.2:c.1899T>G	NP_001341549.1:p.Pro633=
NM_001354621.2:c.1170T>G	NP_001341550.1:p.Pro390=
NM_001354622.2:c.1170T>G	NP_001341551.1:p.Pro390=
NM_001354623.2:c.1170T>G	NP_001341552.1:p.Pro390=
NM_001354624.2:c.1119T>G	NP_001341553.1:p.Pro373=
NM_001354625.2:c.1119T>G	NP_001341554.1:p.Pro373=
NM_001354626.2:c.1119T>G	NP_001341555.1:p.Pro373=
NM_001354627.2:c.1119T>G	NP_001341556.1:p.Pro373=
NM_001354628.2:c.2100T>G	NP_001341557.1:p.Pro700=
NM_001354629.2:c.2094T>G	NP_001341558.1:p.Pro698=
NM_001354630.2:c.2028T>G	NP_001341559.1:p.Pro676=