Canonical Allele Identifier: CA1357864739
Gene: MLH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.36993485G= , CM000665.2:g.36993485G= GRCh38
NC_000003.11:g.37034976G= , CM000665.1:g.37034976G= GRCh37
NC_000003.10:g.37009980G= NCBI36
NG_007109.2:g.5136G= , LRG_216:g.5136G=
NG_008418.1:g.4820C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000413740.2:c.-63G= ENSP00000416476.2:n.-63G=
ENST00000616768.6:c.-63G= ENSP00000480669.3:n.-63G=
ENST00000673673.2:c.-63G= ENSP00000500979.2:n.-63G=
ENST00000231790.6:c.-63G= ENSP00000231790.2:n.-63G=
ENST00000536378.5:c.-695G= ENSP00000444286.2:n.-695G=
NM_000249.3:c.-63G= , LRG_216t1:c.-63G= NP_000240.1:n.-63G=
NM_001258271.1:c.-63G= NP_001245200.1:n.-63G=
NM_001258273.1:c.-695G= NP_001245202.1:n.-695G=
XM_005265161.1:c.-63G= XP_005265218.1:n.-63G=
NM_001167617.2:c.-579G= NP_001161089.1:n.-579G=
NM_001167618.2:c.-1008G= NP_001161090.1:n.-1008G=
NM_001167619.2:c.-921G= NP_001161091.1:n.-921G=
NM_001258274.2:c.-1158G= NP_001245203.1:n.-1158G=
NM_001354615.1:c.-689G= NP_001341544.1:n.-689G=
NM_001354616.1:c.-689G= NP_001341545.1:n.-689G=
NM_001354617.1:c.-781G= NP_001341546.1:n.-781G=
NM_001354618.1:c.-1013G= NP_001341547.1:n.-1013G=
NM_001354619.1:c.-1137G= NP_001341548.1:n.-1137G=
NM_001354620.1:c.-347G= NP_001341549.1:n.-347G=
NM_001354621.1:c.-1106G= NP_001341550.1:n.-1106G=
NM_001354622.1:c.-1219G= NP_001341551.1:n.-1219G=
NM_001354623.1:c.-1128G= NP_001341552.1:n.-1128G=
NM_001354624.1:c.-889G= NP_001341553.1:n.-889G=
NM_001354625.1:c.-787G= NP_001341554.1:n.-787G=
NM_001354626.1:c.-884G= NP_001341555.1:n.-884G=
NM_001354627.1:c.-1116G= NP_001341556.1:n.-1116G=
NM_001354628.1:c.-63G= NP_001341557.1:n.-63G=
NM_001354629.1:c.-63G= NP_001341558.1:n.-63G=
NM_001354630.1:c.-63G= NP_001341559.1:n.-63G=