Canonical Allele Identifier: CA964780764
Gene: MLH3 HGNC NCBI

Linked Data

dbSNP Id: rs1183608204

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75031995G>A , CM000676.2:g.75031995G>A GRCh38
NC_000014.8:g.75498698G>A , CM000676.1:g.75498698G>A GRCh37
NC_000014.7:g.74568451G>A NCBI36
NG_008649.1:g.24538C>T , LRG_217:g.24538C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000355774.7:c.3827+73C>T MANE Select ENSP00000348020.2:n.3827+73C>T
ENST00000355774.6:c.3827+73C>T ENSP00000348020.2:n.3827+73C>T
ENST00000380968.6:c.3755+73C>T ENSP00000370355.3:n.3755+73C>T
ENST00000553713.5:c.898+73C>T
ENST00000555144.5:c.858+73C>T
ENST00000555499.1:n.382+73C>T
ENST00000556257.5:c.3281-1280C>T ENSP00000451540.1:n.3281-1280C>T
ENST00000556453.5:c.372+73C>T
ENST00000556740.5:c.3827+73C>T ENSP00000452316.1:n.3827+73C>T
NM_001040108.1:c.3827+73C>T , LRG_217t1:c.3827+73C>T NP_001035197.1:n.3827+73C>T
NM_014381.2:c.3755+73C>T NP_055196.2:n.3755+73C>T
XM_005267531.3:c.3827+73C>T XP_005267588.1:n.3827+73C>T
XM_005267532.3:c.3722+73C>T XP_005267589.1:n.3722+73C>T
XM_005267533.3:c.3650+73C>T XP_005267590.1:n.3650+73C>T
XM_005267534.2:c.3827+73C>T XP_005267591.1:n.3827+73C>T
XM_006720116.2:c.3827+73C>T XP_006720179.1:n.3827+73C>T
XM_011536646.1:c.3644-1280C>T XP_011534948.1:n.3644-1280C>T
XM_011536647.1:c.3827+73C>T XP_011534949.1:n.3827+73C>T
XR_245681.2:n.4043+73C>T
XM_005267532.5:c.3722+73C>T XP_005267589.1:n.3722+73C>T
XM_005267533.5:c.3650+73C>T XP_005267590.1:n.3650+73C>T
XM_005267534.3:c.3827+73C>T XP_005267591.1:n.3827+73C>T
XM_006720116.4:c.3827+73C>T XP_006720179.1:n.3827+73C>T
XM_011536646.3:c.3644-1280C>T XP_011534948.1:n.3644-1280C>T
XM_017021219.2:c.3755+73C>T XP_016876708.1:n.3755+73C>T
XM_024449538.1:c.3722+73C>T XP_024305306.1:n.3722+73C>T
XM_024449539.1:c.275+73C>T XP_024305307.1:n.275+73C>T
XR_001750225.2:n.3918+73C>T
XR_001750227.2:n.3990+73C>T
XR_001750228.2:n.3990+73C>T
XR_001750229.2:n.3885+73C>T
XR_001750230.2:n.3885+73C>T
XR_002957544.1:n.3999+73C>T
XR_245681.4:n.3990+73C>T
NM_001040108.2:c.3827+73C>T MANE Select NP_001035197.1:n.3827+73C>T
NM_014381.3:c.3755+73C>T NP_055196.2:n.3755+73C>T