Canonical Allele Identifier: CA2147306459

Gene: MLH3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75017093C= , CM000676.2:g.75017093C=	GRCh38
NC_000014.8:g.75483796C= , CM000676.1:g.75483796C=	GRCh37
NC_000014.7:g.74553549C=	NCBI36
NG_008649.1:g.39440G= , LRG_217:g.39440G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001040108.2:c.4351G= MANE Select	NP_001035197.1:p.Glu1451=
ENST00000355774.7:c.4351G= MANE Select	ENSP00000348020.2:p.Glu1451=
NM_001040108.1:c.4351G= , LRG_217t1:c.4351G=	NP_001035197.1:p.Glu1451=
NM_014381.2:c.4279G=	NP_055196.2:p.Glu1427=
NM_014381.3:c.4279G=	NP_055196.2:p.Glu1427=
ENST00000355774.6:c.4351G=	ENSP00000348020.2:p.Glu1451=
ENST00000380968.6:c.4279G=	ENSP00000370355.3:p.Glu1427=
ENST00000553713.5:c.1422G=
ENST00000554697.5:c.364G=	ENSP00000451055.1:p.Glu122=
ENST00000555415.1:n.393G=
ENST00000556257.5:c.3817G=	ENSP00000451540.1:p.Glu1273=
ENST00000556740.5:c.4351G=	ENSP00000452316.1:p.Glu1451=
XM_005267531.3:c.4351G=	XP_005267588.1:p.Glu1451=
XM_005267532.3:c.4246G=	XP_005267589.1:p.Glu1416=
XM_005267532.5:c.4246G=	XP_005267589.1:p.Glu1416=
XM_005267533.3:c.4174G=	XP_005267590.1:p.Glu1392=
XM_005267533.5:c.4174G=	XP_005267590.1:p.Glu1392=
XM_006720116.2:c.4351G=	XP_006720179.1:p.Glu1451=
XM_006720116.4:c.4351G=	XP_006720179.1:p.Glu1451=
XM_011536646.1:c.4180G=	XP_011534948.1:p.Glu1394=
XM_011536646.3:c.4180G=	XP_011534948.1:p.Glu1394=
XM_017021219.2:c.4279G=	XP_016876708.1:p.Glu1427=
XM_024449538.1:c.4246G=	XP_024305306.1:p.Glu1416=
XM_024449539.1:c.799G=	XP_024305307.1:p.Glu267=
XR_001750225.2:n.4442G=
XR_001750227.2:n.4354G=
XR_001750228.2:n.4527G=
XR_001750229.2:n.4422G=
XR_001750230.2:n.4359G=
XR_002957544.1:n.4523G=
XR_245681.2:n.4567G=
XR_245681.4:n.4514G=