Canonical Allele Identifier: CA708529588

Gene: MLH3

Linked Data

• dbSNP Id: rs1183975685
• gnomAD v3: 14-75032008-C-T
• gnomAD v4: 14-75032008-C-T
• MyVariant Identifiers: chr14:g.75498711C>T (hg19) ; chr14:g.75032008C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75032008C>T , CM000676.2:g.75032008C>T	GRCh38
NC_000014.8:g.75498711C>T , CM000676.1:g.75498711C>T	GRCh37
NC_000014.7:g.74568464C>T	NCBI36
NG_008649.1:g.24525G>A , LRG_217:g.24525G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355774.7:c.3827+60G>A MANE Select	ENSP00000348020.2:n.3827+60G>A
ENST00000355774.6:c.3827+60G>A	ENSP00000348020.2:n.3827+60G>A
ENST00000380968.6:c.3755+60G>A	ENSP00000370355.3:n.3755+60G>A
ENST00000553713.5:c.898+60G>A
ENST00000555144.5:c.858+60G>A
ENST00000555499.1:n.382+60G>A
ENST00000556257.5:c.3281-1293G>A	ENSP00000451540.1:n.3281-1293G>A
ENST00000556453.5:c.372+60G>A
ENST00000556740.5:c.3827+60G>A	ENSP00000452316.1:n.3827+60G>A
NM_001040108.1:c.3827+60G>A , LRG_217t1:c.3827+60G>A	NP_001035197.1:n.3827+60G>A
NM_014381.2:c.3755+60G>A	NP_055196.2:n.3755+60G>A
XM_005267531.3:c.3827+60G>A	XP_005267588.1:n.3827+60G>A
XM_005267532.3:c.3722+60G>A	XP_005267589.1:n.3722+60G>A
XM_005267533.3:c.3650+60G>A	XP_005267590.1:n.3650+60G>A
XM_005267534.2:c.3827+60G>A	XP_005267591.1:n.3827+60G>A
XM_006720116.2:c.3827+60G>A	XP_006720179.1:n.3827+60G>A
XM_011536646.1:c.3644-1293G>A	XP_011534948.1:n.3644-1293G>A
XM_011536647.1:c.3827+60G>A	XP_011534949.1:n.3827+60G>A
XR_245681.2:n.4043+60G>A
XM_005267532.5:c.3722+60G>A	XP_005267589.1:n.3722+60G>A
XM_005267533.5:c.3650+60G>A	XP_005267590.1:n.3650+60G>A
XM_005267534.3:c.3827+60G>A	XP_005267591.1:n.3827+60G>A
XM_006720116.4:c.3827+60G>A	XP_006720179.1:n.3827+60G>A
XM_011536646.3:c.3644-1293G>A	XP_011534948.1:n.3644-1293G>A
XM_017021219.2:c.3755+60G>A	XP_016876708.1:n.3755+60G>A
XM_024449538.1:c.3722+60G>A	XP_024305306.1:n.3722+60G>A
XM_024449539.1:c.275+60G>A	XP_024305307.1:n.275+60G>A
XR_001750225.2:n.3918+60G>A
XR_001750227.2:n.3990+60G>A
XR_001750228.2:n.3990+60G>A
XR_001750229.2:n.3885+60G>A
XR_001750230.2:n.3885+60G>A
XR_002957544.1:n.3999+60G>A
XR_245681.4:n.3990+60G>A
NM_001040108.2:c.3827+60G>A MANE Select	NP_001035197.1:n.3827+60G>A
NM_014381.3:c.3755+60G>A	NP_055196.2:n.3755+60G>A