Canonical Allele Identifier: CA007190

Gene: MLH1

Linked Data

• ClinVar Variation Id: 188186
• ClinVar RCV Id: RCV000168095 ; RCV000220697 ; RCV000662568 ; RCV000588543
• dbSNP Id: rs63750449
• gnomAD v4: 3-37047640-A-T
• MyVariant Identifiers: chr3:g.37089131A>T (hg19) ; chr3:g.37047640A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.37047640A>T , CM000665.2:g.37047640A>T	GRCh38
NC_000003.11:g.37089131A>T , CM000665.1:g.37089131A>T	GRCh37
NC_000003.10:g.37064135A>T	NCBI36
NG_007109.2:g.59291A>T , LRG_216:g.59291A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413740.2:c.1668-2846A>T	ENSP00000416476.2:n.1668-2846A>T
ENST00000429117.6:c.1559A>T	ENSP00000407019.2:p.Lys520Met
ENST00000450420.6:c.1559-2846A>T	ENSP00000393006.2:n.1559-2846A>T
ENST00000456676.7:c.1853A>T	ENSP00000416687.3:p.Lys618Met
ENST00000492474.6:c.1130A>T	ENSP00000518393.1:p.Lys377Met
ENST00000616768.6:c.1853A>T	ENSP00000480669.3:p.Lys618Met
ENST00000673673.2:c.1732-877A>T	ENSP00000500979.2:n.1732-877A>T
ENST00000231790.8:c.1853A>T MANE Select	ENSP00000231790.3:p.Lys618Met
ENST00000413212.2:c.*771A>T	ENSP00000400844.2:n.*771A>T
ENST00000432299.6:c.*1685A>T	ENSP00000416783.1:n.*1685A>T
ENST00000441265.6:c.*82A>T	ENSP00000398392.2:n.*82A>T
ENST00000447829.6:c.*964A>T	ENSP00000399329.2:n.*964A>T
ENST00000539477.6:c.1130A>T	ENSP00000443665.1:p.Lys377Met
ENST00000616768.5:c.890A>T	ENSP00000480669.2:p.Lys297Met
ENST00000673673.1:c.1685-877A>T
ENST00000673715.1:c.1853A>T	ENSP00000501301.1:p.Lys618Met
ENST00000673741.1:n.887A>T
ENST00000673889.1:n.1235A>T
ENST00000673897.1:c.*1645A>T	ENSP00000501109.1:n.*1645A>T
ENST00000673899.1:c.1121A>T	ENSP00000501030.1:p.Lys374Met
ENST00000673947.1:c.*1993A>T	ENSP00000501304.1:n.*1993A>T
ENST00000673972.1:c.*1731A>T	ENSP00000501281.1:n.*1731A>T
ENST00000674019.1:c.1130A>T	ENSP00000501081.1:p.Lys377Met
ENST00000674111.1:c.*82A>T	ENSP00000501162.1:n.*82A>T
ENST00000674125.1:n.564A>T
ENST00000231790.6:c.1853A>T	ENSP00000231790.2:p.Lys618Met
ENST00000413740.1:c.291-2846A>T	ENSP00000416476.1:n.291-2846A>T
ENST00000435176.5:c.1559A>T	ENSP00000402564.1:p.Lys520Met
ENST00000450420.5:c.182-2846A>T	ENSP00000393006.1:n.182-2846A>T
ENST00000455445.6:c.1130A>T	ENSP00000398272.2:p.Lys377Met
ENST00000456676.6:c.1828A>T
ENST00000458205.6:c.1130A>T	ENSP00000402667.2:p.Lys377Met
ENST00000536378.5:c.1130A>T	ENSP00000444286.2:p.Lys377Met
ENST00000539477.5:c.1130A>T	ENSP00000443665.1:p.Lys377Met
ENST00000616768.4:c.621A>T
NM_000249.3:c.1853A>T , LRG_216t1:c.1853A>T	NP_000240.1:p.Lys618Met
NM_001167617.1:c.1559A>T	NP_001161089.1:p.Lys520Met
NM_001167618.1:c.1130A>T	NP_001161090.1:p.Lys377Met
NM_001167619.1:c.1130A>T	NP_001161091.1:p.Lys377Met
NM_001258271.1:c.1853A>T	NP_001245200.1:p.Lys618Met
NM_001258273.1:c.1130A>T	NP_001245202.1:p.Lys377Met
NM_001258274.1:c.1130A>T	NP_001245203.1:p.Lys377Met
XM_005265161.1:c.1646A>T	XP_005265218.1:p.Lys549Met
XM_005265163.1:c.1130A>T	XP_005265220.1:p.Lys377Met
XM_005265164.1:c.1130A>T	XP_005265221.1:p.Lys377Met
XM_005265166.1:c.830A>T	XP_005265223.1:p.Lys277Met
XM_011533727.1:c.779A>T	XP_011532029.1:p.Lys260Met
NM_001167617.2:c.1559A>T	NP_001161089.1:p.Lys520Met
NM_001167618.2:c.1130A>T	NP_001161090.1:p.Lys377Met
NM_001167619.2:c.1130A>T	NP_001161091.1:p.Lys377Met
NM_001258274.2:c.1130A>T	NP_001245203.1:p.Lys377Met
NM_001354615.1:c.1130A>T	NP_001341544.1:p.Lys377Met
NM_001354616.1:c.1130A>T	NP_001341545.1:p.Lys377Met
NM_001354617.1:c.1130A>T	NP_001341546.1:p.Lys377Met
NM_001354618.1:c.1130A>T	NP_001341547.1:p.Lys377Met
NM_001354619.1:c.1130A>T	NP_001341548.1:p.Lys377Met
NM_001354620.1:c.1559A>T	NP_001341549.1:p.Lys520Met
NM_001354621.1:c.830A>T	NP_001341550.1:p.Lys277Met
NM_001354622.1:c.830A>T	NP_001341551.1:p.Lys277Met
NM_001354623.1:c.830A>T	NP_001341552.1:p.Lys277Met
NM_001354624.1:c.779A>T	NP_001341553.1:p.Lys260Met
NM_001354625.1:c.779A>T	NP_001341554.1:p.Lys260Met
NM_001354626.1:c.779A>T	NP_001341555.1:p.Lys260Met
NM_001354627.1:c.779A>T	NP_001341556.1:p.Lys260Met
NM_001354628.1:c.1853A>T	NP_001341557.1:p.Lys618Met
NM_001354629.1:c.1754A>T	NP_001341558.1:p.Lys585Met
NM_001354630.1:c.1732-877A>T	NP_001341559.1:n.1732-877A>T
XM_005265161.2:c.1646A>T	XP_005265218.1:p.Lys549Met
XM_017006450.2:c.830A>T	XP_016861939.1:p.Lys277Met
NM_000249.4:c.1853A>T MANE Select	NP_000240.1:p.Lys618Met
NM_001167617.3:c.1559A>T	NP_001161089.1:p.Lys520Met
NM_001167618.3:c.1130A>T	NP_001161090.1:p.Lys377Met
NM_001167619.3:c.1130A>T	NP_001161091.1:p.Lys377Met
NM_001258271.2:c.1853A>T	NP_001245200.1:p.Lys618Met
NM_001258273.2:c.1130A>T	NP_001245202.1:p.Lys377Met
NM_001258274.3:c.1130A>T	NP_001245203.1:p.Lys377Met
NM_001354615.2:c.1130A>T	NP_001341544.1:p.Lys377Met
NM_001354616.2:c.1130A>T	NP_001341545.1:p.Lys377Met
NM_001354617.2:c.1130A>T	NP_001341546.1:p.Lys377Met
NM_001354618.2:c.1130A>T	NP_001341547.1:p.Lys377Met
NM_001354619.2:c.1130A>T	NP_001341548.1:p.Lys377Met
NM_001354620.2:c.1559A>T	NP_001341549.1:p.Lys520Met
NM_001354621.2:c.830A>T	NP_001341550.1:p.Lys277Met
NM_001354622.2:c.830A>T	NP_001341551.1:p.Lys277Met
NM_001354623.2:c.830A>T	NP_001341552.1:p.Lys277Met
NM_001354624.2:c.779A>T	NP_001341553.1:p.Lys260Met
NM_001354625.2:c.779A>T	NP_001341554.1:p.Lys260Met
NM_001354626.2:c.779A>T	NP_001341555.1:p.Lys260Met
NM_001354627.2:c.779A>T	NP_001341556.1:p.Lys260Met
NM_001354628.2:c.1853A>T	NP_001341557.1:p.Lys618Met
NM_001354629.2:c.1754A>T	NP_001341558.1:p.Lys585Met
NM_001354630.2:c.1732-877A>T	NP_001341559.1:n.1732-877A>T