Canonical Allele Identifier: CA1357864740
Gene: MLH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.36993486T= , CM000665.2:g.36993486T= GRCh38
NC_000003.11:g.37034977T= , CM000665.1:g.37034977T= GRCh37
NC_000003.10:g.37009981T= NCBI36
NG_007109.2:g.5137T= , LRG_216:g.5137T=
NG_008418.1:g.4819A=

Transcript Alleles

HGVS Amino-acid change
ENST00000413740.2:c.-62T= ENSP00000416476.2:n.-62T=
ENST00000616768.6:c.-62T= ENSP00000480669.3:n.-62T=
ENST00000673673.2:c.-62T= ENSP00000500979.2:n.-62T=
ENST00000231790.6:c.-62T= ENSP00000231790.2:n.-62T=
ENST00000536378.5:c.-694T= ENSP00000444286.2:n.-694T=
NM_000249.3:c.-62T= , LRG_216t1:c.-62T= NP_000240.1:n.-62T=
NM_001258271.1:c.-62T= NP_001245200.1:n.-62T=
NM_001258273.1:c.-694T= NP_001245202.1:n.-694T=
XM_005265161.1:c.-62T= XP_005265218.1:n.-62T=
NM_001167617.2:c.-578T= NP_001161089.1:n.-578T=
NM_001167618.2:c.-1007T= NP_001161090.1:n.-1007T=
NM_001167619.2:c.-920T= NP_001161091.1:n.-920T=
NM_001258274.2:c.-1157T= NP_001245203.1:n.-1157T=
NM_001354615.1:c.-688T= NP_001341544.1:n.-688T=
NM_001354616.1:c.-688T= NP_001341545.1:n.-688T=
NM_001354617.1:c.-780T= NP_001341546.1:n.-780T=
NM_001354618.1:c.-1012T= NP_001341547.1:n.-1012T=
NM_001354619.1:c.-1136T= NP_001341548.1:n.-1136T=
NM_001354620.1:c.-346T= NP_001341549.1:n.-346T=
NM_001354621.1:c.-1105T= NP_001341550.1:n.-1105T=
NM_001354622.1:c.-1218T= NP_001341551.1:n.-1218T=
NM_001354623.1:c.-1127T= NP_001341552.1:n.-1127T=
NM_001354624.1:c.-888T= NP_001341553.1:n.-888T=
NM_001354625.1:c.-786T= NP_001341554.1:n.-786T=
NM_001354626.1:c.-883T= NP_001341555.1:n.-883T=
NM_001354627.1:c.-1115T= NP_001341556.1:n.-1115T=
NM_001354628.1:c.-62T= NP_001341557.1:n.-62T=
NM_001354629.1:c.-62T= NP_001341558.1:n.-62T=
NM_001354630.1:c.-62T= NP_001341559.1:n.-62T=