Canonical Allele Identifier: CA1357864731
Gene: MLH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.36993467T= , CM000665.2:g.36993467T= GRCh38
NC_000003.11:g.37034958T= , CM000665.1:g.37034958T= GRCh37
NC_000003.10:g.37009962T= NCBI36
NG_007109.2:g.5118T= , LRG_216:g.5118T=
NG_008418.1:g.4838A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000413740.2:c.-81T= ENSP00000416476.2:n.-81T=
ENST00000673673.2:c.-81T= ENSP00000500979.2:n.-81T=
ENST00000231790.6:c.-81T= ENSP00000231790.2:n.-81T=
ENST00000536378.5:c.-713T= ENSP00000444286.2:n.-713T=
NM_000249.3:c.-81T= , LRG_216t1:c.-81T= NP_000240.1:n.-81T=
NM_001258271.1:c.-81T= NP_001245200.1:n.-81T=
NM_001258273.1:c.-713T= NP_001245202.1:n.-713T=
XM_005265161.1:c.-81T= XP_005265218.1:n.-81T=
NM_001167617.2:c.-597T= NP_001161089.1:n.-597T=
NM_001167618.2:c.-1026T= NP_001161090.1:n.-1026T=
NM_001167619.2:c.-939T= NP_001161091.1:n.-939T=
NM_001258274.2:c.-1176T= NP_001245203.1:n.-1176T=
NM_001354615.1:c.-707T= NP_001341544.1:n.-707T=
NM_001354616.1:c.-707T= NP_001341545.1:n.-707T=
NM_001354617.1:c.-799T= NP_001341546.1:n.-799T=
NM_001354618.1:c.-1031T= NP_001341547.1:n.-1031T=
NM_001354619.1:c.-1155T= NP_001341548.1:n.-1155T=
NM_001354620.1:c.-365T= NP_001341549.1:n.-365T=
NM_001354621.1:c.-1124T= NP_001341550.1:n.-1124T=
NM_001354622.1:c.-1237T= NP_001341551.1:n.-1237T=
NM_001354623.1:c.-1146T= NP_001341552.1:n.-1146T=
NM_001354624.1:c.-907T= NP_001341553.1:n.-907T=
NM_001354625.1:c.-805T= NP_001341554.1:n.-805T=
NM_001354626.1:c.-902T= NP_001341555.1:n.-902T=
NM_001354627.1:c.-1134T= NP_001341556.1:n.-1134T=
NM_001354628.1:c.-81T= NP_001341557.1:n.-81T=
NM_001354629.1:c.-81T= NP_001341558.1:n.-81T=
NM_001354630.1:c.-81T= NP_001341559.1:n.-81T=