Canonical Allele Identifier: CA008112

Gene: MLH1

Linked Data

• ClinVar Variation Id: 17088
• ClinVar RCV Id: RCV001267885 ; RCV002415421 ; RCV000018618 ; RCV000075475
• dbSNP Id: rs63750206
• COSMIC: COSM1043967
• MyVariant Identifiers: chr3:g.37038192G>T (hg19) ; chr3:g.36996701G>T (hg38)
• PubMed: PMID:9927034 ; PMID:10480359 ; PMID:16042583 ; PMID:16971051 ; PMID:17510385

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.36996701G>T , CM000665.2:g.36996701G>T	GRCh38
NC_000003.11:g.37038192G>T , CM000665.1:g.37038192G>T	GRCh37
NC_000003.10:g.37013196G>T	NCBI36
NG_007109.2:g.8352G>T , LRG_216:g.8352G>T
NG_008418.1:g.1604C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413740.2:c.199G>T	ENSP00000416476.2:p.Gly67Trp
ENST00000429117.6:c.-91G>T	ENSP00000407019.2:n.-91G>T
ENST00000450420.6:c.199G>T	ENSP00000393006.2:p.Gly67Trp
ENST00000456676.7:c.199G>T	ENSP00000416687.3:p.Gly67Trp
ENST00000458009.6:c.199G>T	ENSP00000411066.2:p.Gly67Trp
ENST00000492474.6:c.-525G>T	ENSP00000518393.1:n.-525G>T
ENST00000616768.6:c.199G>T	ENSP00000480669.3:p.Gly67Trp
ENST00000673673.2:c.199G>T	ENSP00000500979.2:p.Gly67Trp
ENST00000231790.8:c.199G>T MANE Select	ENSP00000231790.3:p.Gly67Trp
ENST00000413212.2:c.-525G>T	ENSP00000400844.2:n.-525G>T
ENST00000432299.6:c.*279G>T	ENSP00000416783.1:n.*279G>T
ENST00000441265.6:c.-525G>T	ENSP00000398392.2:n.-525G>T
ENST00000442249.6:n.214G>T
ENST00000447829.6:c.-91G>T	ENSP00000399329.2:n.-91G>T
ENST00000476172.6:n.1120-1269G>T
ENST00000539477.6:c.-433G>T	ENSP00000443665.1:n.-433G>T
ENST00000673673.1:c.152G>T
ENST00000673686.1:n.189G>T
ENST00000673713.1:n.230G>T
ENST00000673715.1:c.199G>T	ENSP00000501301.1:p.Gly67Trp
ENST00000673897.1:c.116+3038G>T	ENSP00000501109.1:n.116+3038G>T
ENST00000673899.1:c.199G>T	ENSP00000501030.1:p.Gly67Trp
ENST00000673947.1:c.*339G>T	ENSP00000501304.1:n.*339G>T
ENST00000673972.1:c.*77G>T	ENSP00000501281.1:n.*77G>T
ENST00000673990.1:n.184G>T
ENST00000674019.1:c.-525G>T	ENSP00000501081.1:n.-525G>T
ENST00000674107.1:n.141G>T
ENST00000674111.1:c.199G>T	ENSP00000501162.1:p.Gly67Trp
ENST00000231790.6:c.199G>T	ENSP00000231790.2:p.Gly67Trp
ENST00000429117.5:c.-91G>T	ENSP00000407019.1:n.-91G>T
ENST00000432299.5:c.*279G>T	ENSP00000416783.1:n.*279G>T
ENST00000435176.5:c.-91G>T	ENSP00000402564.1:n.-91G>T
ENST00000441265.5:c.-433G>T	ENSP00000398392.1:n.-433G>T
ENST00000442249.5:c.116+3038G>T	ENSP00000387511.1:n.116+3038G>T
ENST00000454028.5:c.*77G>T	ENSP00000392649.1:n.*77G>T
ENST00000455445.6:c.-525G>T	ENSP00000398272.2:n.-525G>T
ENST00000456676.6:c.174G>T
ENST00000457004.5:c.*77G>T	ENSP00000407773.1:n.*77G>T
ENST00000458205.6:c.-670G>T	ENSP00000402667.2:n.-670G>T
ENST00000466900.5:n.126G>T
ENST00000476172.5:n.321G>T
ENST00000485889.1:n.203G>T
ENST00000492474.5:n.222G>T
ENST00000536378.5:c.-517+3038G>T	ENSP00000444286.2:n.-517+3038G>T
ENST00000539477.5:c.-433G>T	ENSP00000443665.1:n.-433G>T
NM_000249.3:c.199G>T , LRG_216t1:c.199G>T	NP_000240.1:p.Gly67Trp
NM_001167617.1:c.-91G>T	NP_001161089.1:n.-91G>T
NM_001167618.1:c.-525G>T	NP_001161090.1:n.-525G>T
NM_001167619.1:c.-433G>T	NP_001161091.1:n.-433G>T
NM_001258271.1:c.199G>T	NP_001245200.1:p.Gly67Trp
NM_001258273.1:c.-517+3038G>T	NP_001245202.1:n.-517+3038G>T
NM_001258274.1:c.-670G>T	NP_001245203.1:n.-670G>T
XM_005265161.1:c.199G>T	XP_005265218.1:p.Gly67Trp
XM_005265163.1:c.-525G>T	XP_005265220.1:n.-525G>T
XM_005265164.1:c.-525G>T	XP_005265221.1:n.-525G>T
XM_005265166.1:c.-731G>T	XP_005265223.1:n.-731G>T
XM_011533727.1:c.-628G>T	XP_011532029.1:n.-628G>T
NM_001167617.2:c.-91G>T	NP_001161089.1:n.-91G>T
NM_001167618.2:c.-525G>T	NP_001161090.1:n.-525G>T
NM_001167619.2:c.-433G>T	NP_001161091.1:n.-433G>T
NM_001258274.2:c.-670G>T	NP_001245203.1:n.-670G>T
NM_001354615.1:c.-428G>T	NP_001341544.1:n.-428G>T
NM_001354616.1:c.-433G>T	NP_001341545.1:n.-433G>T
NM_001354617.1:c.-525G>T	NP_001341546.1:n.-525G>T
NM_001354618.1:c.-525G>T	NP_001341547.1:n.-525G>T
NM_001354619.1:c.-525G>T	NP_001341548.1:n.-525G>T
NM_001354620.1:c.-91G>T	NP_001341549.1:n.-91G>T
NM_001354621.1:c.-618G>T	NP_001341550.1:n.-618G>T
NM_001354622.1:c.-731G>T	NP_001341551.1:n.-731G>T
NM_001354623.1:c.-723+2811G>T	NP_001341552.1:n.-723+2811G>T
NM_001354624.1:c.-628G>T	NP_001341553.1:n.-628G>T
NM_001354625.1:c.-531G>T	NP_001341554.1:n.-531G>T
NM_001354626.1:c.-628G>T	NP_001341555.1:n.-628G>T
NM_001354627.1:c.-628G>T	NP_001341556.1:n.-628G>T
NM_001354628.1:c.199G>T	NP_001341557.1:p.Gly67Trp
NM_001354629.1:c.199G>T	NP_001341558.1:p.Gly67Trp
NM_001354630.1:c.199G>T	NP_001341559.1:p.Gly67Trp
XM_005265161.2:c.199G>T	XP_005265218.1:p.Gly67Trp
XM_017006450.2:c.-618G>T	XP_016861939.1:n.-618G>T
NM_000249.4:c.199G>T MANE Select	NP_000240.1:p.Gly67Trp
NM_001167617.3:c.-91G>T	NP_001161089.1:n.-91G>T
NM_001167618.3:c.-525G>T	NP_001161090.1:n.-525G>T
NM_001167619.3:c.-433G>T	NP_001161091.1:n.-433G>T
NM_001258271.2:c.199G>T	NP_001245200.1:p.Gly67Trp
NM_001258273.2:c.-517+3038G>T	NP_001245202.1:n.-517+3038G>T
NM_001258274.3:c.-670G>T	NP_001245203.1:n.-670G>T
NM_001354615.2:c.-428G>T	NP_001341544.1:n.-428G>T
NM_001354616.2:c.-433G>T	NP_001341545.1:n.-433G>T
NM_001354617.2:c.-525G>T	NP_001341546.1:n.-525G>T
NM_001354618.2:c.-525G>T	NP_001341547.1:n.-525G>T
NM_001354619.2:c.-525G>T	NP_001341548.1:n.-525G>T
NM_001354620.2:c.-91G>T	NP_001341549.1:n.-91G>T
NM_001354621.2:c.-618G>T	NP_001341550.1:n.-618G>T
NM_001354622.2:c.-731G>T	NP_001341551.1:n.-731G>T
NM_001354623.2:c.-723+2811G>T	NP_001341552.1:n.-723+2811G>T
NM_001354624.2:c.-628G>T	NP_001341553.1:n.-628G>T
NM_001354625.2:c.-531G>T	NP_001341554.1:n.-531G>T
NM_001354626.2:c.-628G>T	NP_001341555.1:n.-628G>T
NM_001354627.2:c.-628G>T	NP_001341556.1:n.-628G>T
NM_001354628.2:c.199G>T	NP_001341557.1:p.Gly67Trp
NM_001354629.2:c.199G>T	NP_001341558.1:p.Gly67Trp
NM_001354630.2:c.199G>T	NP_001341559.1:p.Gly67Trp