Canonical Allele Identifier: CA1357864736
Gene: MLH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.36993478C= , CM000665.2:g.36993478C= GRCh38
NC_000003.11:g.37034969C= , CM000665.1:g.37034969C= GRCh37
NC_000003.10:g.37009973C= NCBI36
NG_007109.2:g.5129C= , LRG_216:g.5129C=
NG_008418.1:g.4827G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000413740.2:c.-70C= ENSP00000416476.2:n.-70C=
ENST00000616768.6:c.-70C= ENSP00000480669.3:n.-70C=
ENST00000673673.2:c.-70C= ENSP00000500979.2:n.-70C=
ENST00000231790.6:c.-70C= ENSP00000231790.2:n.-70C=
ENST00000536378.5:c.-702C= ENSP00000444286.2:n.-702C=
NM_000249.3:c.-70C= , LRG_216t1:c.-70C= NP_000240.1:n.-70C=
NM_001258271.1:c.-70C= NP_001245200.1:n.-70C=
NM_001258273.1:c.-702C= NP_001245202.1:n.-702C=
XM_005265161.1:c.-70C= XP_005265218.1:n.-70C=
NM_001167617.2:c.-586C= NP_001161089.1:n.-586C=
NM_001167618.2:c.-1015C= NP_001161090.1:n.-1015C=
NM_001167619.2:c.-928C= NP_001161091.1:n.-928C=
NM_001258274.2:c.-1165C= NP_001245203.1:n.-1165C=
NM_001354615.1:c.-696C= NP_001341544.1:n.-696C=
NM_001354616.1:c.-696C= NP_001341545.1:n.-696C=
NM_001354617.1:c.-788C= NP_001341546.1:n.-788C=
NM_001354618.1:c.-1020C= NP_001341547.1:n.-1020C=
NM_001354619.1:c.-1144C= NP_001341548.1:n.-1144C=
NM_001354620.1:c.-354C= NP_001341549.1:n.-354C=
NM_001354621.1:c.-1113C= NP_001341550.1:n.-1113C=
NM_001354622.1:c.-1226C= NP_001341551.1:n.-1226C=
NM_001354623.1:c.-1135C= NP_001341552.1:n.-1135C=
NM_001354624.1:c.-896C= NP_001341553.1:n.-896C=
NM_001354625.1:c.-794C= NP_001341554.1:n.-794C=
NM_001354626.1:c.-891C= NP_001341555.1:n.-891C=
NM_001354627.1:c.-1123C= NP_001341556.1:n.-1123C=
NM_001354628.1:c.-70C= NP_001341557.1:n.-70C=
NM_001354629.1:c.-70C= NP_001341558.1:n.-70C=
NM_001354630.1:c.-70C= NP_001341559.1:n.-70C=