Canonical Allele Identifier: CA2147303691

Gene: MLH3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75031999T= , CM000676.2:g.75031999T=	GRCh38
NC_000014.8:g.75498702T= , CM000676.1:g.75498702T=	GRCh37
NC_000014.7:g.74568455T=	NCBI36
NG_008649.1:g.24534A= , LRG_217:g.24534A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355774.7:c.3827+69A= MANE Select	ENSP00000348020.2:n.3827+69A=
ENST00000355774.6:c.3827+69A=	ENSP00000348020.2:n.3827+69A=
ENST00000380968.6:c.3755+69A=	ENSP00000370355.3:n.3755+69A=
ENST00000553713.5:c.898+69A=
ENST00000555144.5:c.858+69A=
ENST00000555499.1:n.382+69A=
ENST00000556257.5:c.3281-1284A=	ENSP00000451540.1:n.3281-1284A=
ENST00000556453.5:c.372+69A=
ENST00000556740.5:c.3827+69A=	ENSP00000452316.1:n.3827+69A=
NM_001040108.1:c.3827+69A= , LRG_217t1:c.3827+69A=	NP_001035197.1:n.3827+69A=
NM_014381.2:c.3755+69A=	NP_055196.2:n.3755+69A=
XM_005267531.3:c.3827+69A=	XP_005267588.1:n.3827+69A=
XM_005267532.3:c.3722+69A=	XP_005267589.1:n.3722+69A=
XM_005267533.3:c.3650+69A=	XP_005267590.1:n.3650+69A=
XM_005267534.2:c.3827+69A=	XP_005267591.1:n.3827+69A=
XM_006720116.2:c.3827+69A=	XP_006720179.1:n.3827+69A=
XM_011536646.1:c.3644-1284A=	XP_011534948.1:n.3644-1284A=
XM_011536647.1:c.3827+69A=	XP_011534949.1:n.3827+69A=
XR_245681.2:n.4043+69A=
XM_005267532.5:c.3722+69A=	XP_005267589.1:n.3722+69A=
XM_005267533.5:c.3650+69A=	XP_005267590.1:n.3650+69A=
XM_005267534.3:c.3827+69A=	XP_005267591.1:n.3827+69A=
XM_006720116.4:c.3827+69A=	XP_006720179.1:n.3827+69A=
XM_011536646.3:c.3644-1284A=	XP_011534948.1:n.3644-1284A=
XM_017021219.2:c.3755+69A=	XP_016876708.1:n.3755+69A=
XM_024449538.1:c.3722+69A=	XP_024305306.1:n.3722+69A=
XM_024449539.1:c.275+69A=	XP_024305307.1:n.275+69A=
XR_001750225.2:n.3918+69A=
XR_001750227.2:n.3990+69A=
XR_001750228.2:n.3990+69A=
XR_001750229.2:n.3885+69A=
XR_001750230.2:n.3885+69A=
XR_002957544.1:n.3999+69A=
XR_245681.4:n.3990+69A=
NM_001040108.2:c.3827+69A= MANE Select	NP_001035197.1:n.3827+69A=
NM_014381.3:c.3755+69A=	NP_055196.2:n.3755+69A=