Canonical Allele Identifier: CA352065037

Gene: MLH1

Linked Data

• MyVariant Identifiers: chr3:g.37089116A>C (hg19) ; chr3:g.37047625A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.37047625A>C , CM000665.2:g.37047625A>C	GRCh38
NC_000003.11:g.37089116A>C , CM000665.1:g.37089116A>C	GRCh37
NC_000003.10:g.37064120A>C	NCBI36
NG_007109.2:g.59276A>C , LRG_216:g.59276A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413740.2:c.1668-2861A>C	ENSP00000416476.2:n.1668-2861A>C
ENST00000429117.6:c.1544A>C	ENSP00000407019.2:p.Glu515Ala
ENST00000450420.6:c.1559-2861A>C	ENSP00000393006.2:n.1559-2861A>C
ENST00000456676.7:c.1838A>C	ENSP00000416687.3:p.Glu613Ala
ENST00000492474.6:c.1115A>C	ENSP00000518393.1:p.Glu372Ala
ENST00000616768.6:c.1838A>C	ENSP00000480669.3:p.Glu613Ala
ENST00000673673.2:c.1732-892A>C	ENSP00000500979.2:n.1732-892A>C
ENST00000231790.8:c.1838A>C MANE Select	ENSP00000231790.3:p.Glu613Ala
ENST00000413212.2:c.*756A>C	ENSP00000400844.2:n.*756A>C
ENST00000432299.6:c.*1670A>C	ENSP00000416783.1:n.*1670A>C
ENST00000441265.6:c.*67A>C	ENSP00000398392.2:n.*67A>C
ENST00000447829.6:c.*949A>C	ENSP00000399329.2:n.*949A>C
ENST00000539477.6:c.1115A>C	ENSP00000443665.1:p.Glu372Ala
ENST00000616768.5:c.875A>C	ENSP00000480669.2:p.Glu292Ala
ENST00000673673.1:c.1685-892A>C
ENST00000673715.1:c.1838A>C	ENSP00000501301.1:p.Glu613Ala
ENST00000673741.1:n.872A>C
ENST00000673889.1:n.1220A>C
ENST00000673897.1:c.*1630A>C	ENSP00000501109.1:n.*1630A>C
ENST00000673899.1:c.1106A>C	ENSP00000501030.1:p.Glu369Ala
ENST00000673947.1:c.*1978A>C	ENSP00000501304.1:n.*1978A>C
ENST00000673972.1:c.*1716A>C	ENSP00000501281.1:n.*1716A>C
ENST00000674019.1:c.1115A>C	ENSP00000501081.1:p.Glu372Ala
ENST00000674111.1:c.*67A>C	ENSP00000501162.1:n.*67A>C
ENST00000674125.1:n.549A>C
ENST00000231790.6:c.1838A>C	ENSP00000231790.2:p.Glu613Ala
ENST00000413740.1:c.291-2861A>C	ENSP00000416476.1:n.291-2861A>C
ENST00000435176.5:c.1544A>C	ENSP00000402564.1:p.Glu515Ala
ENST00000450420.5:c.182-2861A>C	ENSP00000393006.1:n.182-2861A>C
ENST00000455445.6:c.1115A>C	ENSP00000398272.2:p.Glu372Ala
ENST00000456676.6:c.1813A>C
ENST00000458205.6:c.1115A>C	ENSP00000402667.2:p.Glu372Ala
ENST00000536378.5:c.1115A>C	ENSP00000444286.2:p.Glu372Ala
ENST00000539477.5:c.1115A>C	ENSP00000443665.1:p.Glu372Ala
ENST00000616768.4:c.606A>C
NM_000249.3:c.1838A>C , LRG_216t1:c.1838A>C	NP_000240.1:p.Glu613Ala
NM_001167617.1:c.1544A>C	NP_001161089.1:p.Glu515Ala
NM_001167618.1:c.1115A>C	NP_001161090.1:p.Glu372Ala
NM_001167619.1:c.1115A>C	NP_001161091.1:p.Glu372Ala
NM_001258271.1:c.1838A>C	NP_001245200.1:p.Glu613Ala
NM_001258273.1:c.1115A>C	NP_001245202.1:p.Glu372Ala
NM_001258274.1:c.1115A>C	NP_001245203.1:p.Glu372Ala
XM_005265161.1:c.1631A>C	XP_005265218.1:p.Glu544Ala
XM_005265163.1:c.1115A>C	XP_005265220.1:p.Glu372Ala
XM_005265164.1:c.1115A>C	XP_005265221.1:p.Glu372Ala
XM_005265166.1:c.815A>C	XP_005265223.1:p.Glu272Ala
XM_011533727.1:c.764A>C	XP_011532029.1:p.Glu255Ala
NM_001167617.2:c.1544A>C	NP_001161089.1:p.Glu515Ala
NM_001167618.2:c.1115A>C	NP_001161090.1:p.Glu372Ala
NM_001167619.2:c.1115A>C	NP_001161091.1:p.Glu372Ala
NM_001258274.2:c.1115A>C	NP_001245203.1:p.Glu372Ala
NM_001354615.1:c.1115A>C	NP_001341544.1:p.Glu372Ala
NM_001354616.1:c.1115A>C	NP_001341545.1:p.Glu372Ala
NM_001354617.1:c.1115A>C	NP_001341546.1:p.Glu372Ala
NM_001354618.1:c.1115A>C	NP_001341547.1:p.Glu372Ala
NM_001354619.1:c.1115A>C	NP_001341548.1:p.Glu372Ala
NM_001354620.1:c.1544A>C	NP_001341549.1:p.Glu515Ala
NM_001354621.1:c.815A>C	NP_001341550.1:p.Glu272Ala
NM_001354622.1:c.815A>C	NP_001341551.1:p.Glu272Ala
NM_001354623.1:c.815A>C	NP_001341552.1:p.Glu272Ala
NM_001354624.1:c.764A>C	NP_001341553.1:p.Glu255Ala
NM_001354625.1:c.764A>C	NP_001341554.1:p.Glu255Ala
NM_001354626.1:c.764A>C	NP_001341555.1:p.Glu255Ala
NM_001354627.1:c.764A>C	NP_001341556.1:p.Glu255Ala
NM_001354628.1:c.1838A>C	NP_001341557.1:p.Glu613Ala
NM_001354629.1:c.1739A>C	NP_001341558.1:p.Glu580Ala
NM_001354630.1:c.1732-892A>C	NP_001341559.1:n.1732-892A>C
XM_005265161.2:c.1631A>C	XP_005265218.1:p.Glu544Ala
XM_017006450.2:c.815A>C	XP_016861939.1:p.Glu272Ala
NM_000249.4:c.1838A>C MANE Select	NP_000240.1:p.Glu613Ala
NM_001167617.3:c.1544A>C	NP_001161089.1:p.Glu515Ala
NM_001167618.3:c.1115A>C	NP_001161090.1:p.Glu372Ala
NM_001167619.3:c.1115A>C	NP_001161091.1:p.Glu372Ala
NM_001258271.2:c.1838A>C	NP_001245200.1:p.Glu613Ala
NM_001258273.2:c.1115A>C	NP_001245202.1:p.Glu372Ala
NM_001258274.3:c.1115A>C	NP_001245203.1:p.Glu372Ala
NM_001354615.2:c.1115A>C	NP_001341544.1:p.Glu372Ala
NM_001354616.2:c.1115A>C	NP_001341545.1:p.Glu372Ala
NM_001354617.2:c.1115A>C	NP_001341546.1:p.Glu372Ala
NM_001354618.2:c.1115A>C	NP_001341547.1:p.Glu372Ala
NM_001354619.2:c.1115A>C	NP_001341548.1:p.Glu372Ala
NM_001354620.2:c.1544A>C	NP_001341549.1:p.Glu515Ala
NM_001354621.2:c.815A>C	NP_001341550.1:p.Glu272Ala
NM_001354622.2:c.815A>C	NP_001341551.1:p.Glu272Ala
NM_001354623.2:c.815A>C	NP_001341552.1:p.Glu272Ala
NM_001354624.2:c.764A>C	NP_001341553.1:p.Glu255Ala
NM_001354625.2:c.764A>C	NP_001341554.1:p.Glu255Ala
NM_001354626.2:c.764A>C	NP_001341555.1:p.Glu255Ala
NM_001354627.2:c.764A>C	NP_001341556.1:p.Glu255Ala
NM_001354628.2:c.1838A>C	NP_001341557.1:p.Glu613Ala
NM_001354629.2:c.1739A>C	NP_001341558.1:p.Glu580Ala
NM_001354630.2:c.1732-892A>C	NP_001341559.1:n.1732-892A>C