Canonical Allele Identifier: CA2147303743
Community Standard Title: NM_001040108.2(MLH3):c.3826T= (p.Trp1276=)
Gene: MLH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75032069A= , CM000676.2:g.75032069A= GRCh38
NC_000014.8:g.75498772A= , CM000676.1:g.75498772A= GRCh37
NC_000014.7:g.74568525A= NCBI36
NG_008649.1:g.24464T= , LRG_217:g.24464T=

Transcript Alleles

HGVS Amino-acid Change
NM_001040108.2:c.3826T= MANE Select NP_001035197.1:p.Trp1276=
ENST00000355774.7:c.3826T= MANE Select ENSP00000348020.2:p.Trp1276=
NM_001040108.1:c.3826T= , LRG_217t1:c.3826T= NP_001035197.1:p.Trp1276=
NM_014381.2:c.3754T= NP_055196.2:p.Trp1252=
NM_014381.3:c.3754T= NP_055196.2:p.Trp1252=
ENST00000355774.6:c.3826T= ENSP00000348020.2:p.Trp1276=
ENST00000380968.6:c.3754T= ENSP00000370355.3:p.Trp1252=
ENST00000553713.5:c.897T=
ENST00000555144.5:c.857T=
ENST00000555499.1:n.381T=
ENST00000556257.5:c.3281-1354T= ENSP00000451540.1:n.3281-1354T=
ENST00000556453.5:c.371T=
ENST00000556740.5:c.3826T= ENSP00000452316.1:p.Trp1276=
XM_005267531.3:c.3826T= XP_005267588.1:p.Trp1276=
XM_005267532.3:c.3721T= XP_005267589.1:p.Trp1241=
XM_005267532.5:c.3721T= XP_005267589.1:p.Trp1241=
XM_005267533.3:c.3649T= XP_005267590.1:p.Trp1217=
XM_005267533.5:c.3649T= XP_005267590.1:p.Trp1217=
XM_005267534.2:c.3826T= XP_005267591.1:p.Ter1276=
XM_005267534.3:c.3826T= XP_005267591.1:p.Ter1276=
XM_006720116.2:c.3826T= XP_006720179.1:p.Trp1276=
XM_006720116.4:c.3826T= XP_006720179.1:p.Trp1276=
XM_011536646.1:c.3644-1354T= XP_011534948.1:n.3644-1354T=
XM_011536646.3:c.3644-1354T= XP_011534948.1:n.3644-1354T=
XM_011536647.1:c.3826T= XP_011534949.1:p.Trp1276=
XM_017021219.2:c.3754T= XP_016876708.1:p.Trp1252=
XM_024449538.1:c.3721T= XP_024305306.1:p.Trp1241=
XM_024449539.1:c.274T= XP_024305307.1:p.Trp92=
XR_001750225.2:n.3917T=
XR_001750227.2:n.3989T=
XR_001750228.2:n.3989T=
XR_001750229.2:n.3884T=
XR_001750230.2:n.3884T=
XR_002957544.1:n.3998T=
XR_245681.2:n.4042T=
XR_245681.4:n.3989T=