Canonical Allele Identifier: CA1357864729
Gene: MLH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.36993462G= , CM000665.2:g.36993462G= GRCh38
NC_000003.11:g.37034953G= , CM000665.1:g.37034953G= GRCh37
NC_000003.10:g.37009957G= NCBI36
NG_007109.2:g.5113G= , LRG_216:g.5113G=
NG_008418.1:g.4843C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000413740.2:c.-86G= ENSP00000416476.2:n.-86G=
ENST00000673673.2:c.-86G= ENSP00000500979.2:n.-86G=
ENST00000231790.6:c.-86G= ENSP00000231790.2:n.-86G=
ENST00000536378.5:c.-718G= ENSP00000444286.2:n.-718G=
NM_000249.3:c.-86G= , LRG_216t1:c.-86G= NP_000240.1:n.-86G=
NM_001258271.1:c.-86G= NP_001245200.1:n.-86G=
NM_001258273.1:c.-718G= NP_001245202.1:n.-718G=
XM_005265161.1:c.-86G= XP_005265218.1:n.-86G=
NM_001167617.2:c.-602G= NP_001161089.1:n.-602G=
NM_001167618.2:c.-1031G= NP_001161090.1:n.-1031G=
NM_001167619.2:c.-944G= NP_001161091.1:n.-944G=
NM_001258274.2:c.-1181G= NP_001245203.1:n.-1181G=
NM_001354615.1:c.-712G= NP_001341544.1:n.-712G=
NM_001354616.1:c.-712G= NP_001341545.1:n.-712G=
NM_001354617.1:c.-804G= NP_001341546.1:n.-804G=
NM_001354618.1:c.-1036G= NP_001341547.1:n.-1036G=
NM_001354619.1:c.-1160G= NP_001341548.1:n.-1160G=
NM_001354620.1:c.-370G= NP_001341549.1:n.-370G=
NM_001354621.1:c.-1129G= NP_001341550.1:n.-1129G=
NM_001354622.1:c.-1242G= NP_001341551.1:n.-1242G=
NM_001354623.1:c.-1151G= NP_001341552.1:n.-1151G=
NM_001354624.1:c.-912G= NP_001341553.1:n.-912G=
NM_001354625.1:c.-810G= NP_001341554.1:n.-810G=
NM_001354626.1:c.-907G= NP_001341555.1:n.-907G=
NM_001354627.1:c.-1139G= NP_001341556.1:n.-1139G=
NM_001354628.1:c.-86G= NP_001341557.1:n.-86G=
NM_001354629.1:c.-86G= NP_001341558.1:n.-86G=
NM_001354630.1:c.-86G= NP_001341559.1:n.-86G=