Canonical Allele Identifier: CA2147317531
Gene: MLH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75047221C= , CM000676.2:g.75047221C= GRCh38
NC_000014.8:g.75513924C= , CM000676.1:g.75513924C= GRCh37
NC_000014.7:g.74583677C= NCBI36
NG_008649.1:g.9312G= , LRG_217:g.9312G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355774.7:c.2435G= MANE Select ENSP00000348020.2:p.Ser812=
ENST00000355774.6:c.2435G= ENSP00000348020.2:p.Ser812=
ENST00000380968.6:c.2435G= ENSP00000370355.3:p.Ser812=
ENST00000556257.5:c.2435G= ENSP00000451540.1:p.Ser812=
ENST00000556740.5:c.2435G= ENSP00000452316.1:p.Ser812=
NM_001040108.1:c.2435G= , LRG_217t1:c.2435G= NP_001035197.1:p.Ser812=
NM_014381.2:c.2435G= NP_055196.2:p.Ser812=
XM_005267531.3:c.2435G= XP_005267588.1:p.Ser812=
XM_005267532.3:c.2435G= XP_005267589.1:p.Ser812=
XM_005267533.3:c.2435G= XP_005267590.1:p.Ser812=
XM_005267534.2:c.2435G= XP_005267591.1:p.Ser812=
XM_006720116.2:c.2435G= XP_006720179.1:p.Ser812=
XM_011536646.1:c.2435G= XP_011534948.1:p.Ser812=
XM_011536647.1:c.2435G= XP_011534949.1:p.Ser812=
XM_011536648.1:c.2435G= XP_011534950.1:p.Ser812=
XR_245681.2:n.2651G=
XM_005267532.5:c.2435G= XP_005267589.1:p.Ser812=
XM_005267533.5:c.2435G= XP_005267590.1:p.Ser812=
XM_005267534.3:c.2435G= XP_005267591.1:p.Ser812=
XM_006720116.4:c.2435G= XP_006720179.1:p.Ser812=
XM_011536646.3:c.2435G= XP_011534948.1:p.Ser812=
XM_017021219.2:c.2435G= XP_016876708.1:p.Ser812=
XM_024449538.1:c.2435G= XP_024305306.1:p.Ser812=
XR_001750225.2:n.2598G=
XR_001750227.2:n.2598G=
XR_001750228.2:n.2598G=
XR_001750229.2:n.2598G=
XR_001750230.2:n.2598G=
XR_002957544.1:n.2598G=
XR_245681.4:n.2598G=
NM_001040108.2:c.2435G= MANE Select NP_001035197.1:p.Ser812=
NM_014381.3:c.2435G= NP_055196.2:p.Ser812=