Canonical Allele Identifier: CA2625719915

Gene: MLH3

Linked Data

• gnomAD v4: 14-75031987-GAACAATAGTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75031989_75031998del , CM000676.2:g.75031989_75031998del	GRCh38
NC_000014.8:g.75498692_75498701del , CM000676.1:g.75498692_75498701del	GRCh37
NC_000014.7:g.74568445_74568454del	NCBI36
NG_008649.1:g.24536_24545del , LRG_217:g.24536_24545del

Transcript Alleles

HGVS	Amino-acid change
ENST00000355774.7:c.3827+71_3827+80del MANE Select	ENSP00000348020.2:n.3827+71_3827+80del
ENST00000355774.6:c.3827+71_3827+80del	ENSP00000348020.2:n.3827+71_3827+80del
ENST00000380968.6:c.3755+71_3755+80del	ENSP00000370355.3:n.3755+71_3755+80del
ENST00000553713.5:c.898+71_898+80del
ENST00000555144.5:c.858+71_858+80del
ENST00000555499.1:n.382+71_382+80del
ENST00000556257.5:c.3281-1282_3281-1273del	ENSP00000451540.1:n.3281-1282_3281-1273del
ENST00000556453.5:c.372+71_372+80del
ENST00000556740.5:c.3827+71_3827+80del	ENSP00000452316.1:n.3827+71_3827+80del
NM_001040108.1:c.3827+71_3827+80del , LRG_217t1:c.3827+71_3827+80del	NP_001035197.1:n.3827+71_3827+80del
NM_014381.2:c.3755+71_3755+80del	NP_055196.2:n.3755+71_3755+80del
XM_005267531.3:c.3827+71_3827+80del	XP_005267588.1:n.3827+71_3827+80del
XM_005267532.3:c.3722+71_3722+80del	XP_005267589.1:n.3722+71_3722+80del
XM_005267533.3:c.3650+71_3650+80del	XP_005267590.1:n.3650+71_3650+80del
XM_005267534.2:c.3827+71_3827+80del	XP_005267591.1:n.3827+71_3827+80del
XM_006720116.2:c.3827+71_3827+80del	XP_006720179.1:n.3827+71_3827+80del
XM_011536646.1:c.3644-1282_3644-1273del	XP_011534948.1:n.3644-1282_3644-1273del
XM_011536647.1:c.3827+71_3827+80del	XP_011534949.1:n.3827+71_3827+80del
XR_245681.2:n.4043+71_4043+80del
XM_005267532.5:c.3722+71_3722+80del	XP_005267589.1:n.3722+71_3722+80del
XM_005267533.5:c.3650+71_3650+80del	XP_005267590.1:n.3650+71_3650+80del
XM_005267534.3:c.3827+71_3827+80del	XP_005267591.1:n.3827+71_3827+80del
XM_006720116.4:c.3827+71_3827+80del	XP_006720179.1:n.3827+71_3827+80del
XM_011536646.3:c.3644-1282_3644-1273del	XP_011534948.1:n.3644-1282_3644-1273del
XM_017021219.2:c.3755+71_3755+80del	XP_016876708.1:n.3755+71_3755+80del
XM_024449538.1:c.3722+71_3722+80del	XP_024305306.1:n.3722+71_3722+80del
XM_024449539.1:c.275+71_275+80del	XP_024305307.1:n.275+71_275+80del
XR_001750225.2:n.3918+71_3918+80del
XR_001750227.2:n.3990+71_3990+80del
XR_001750228.2:n.3990+71_3990+80del
XR_001750229.2:n.3885+71_3885+80del
XR_001750230.2:n.3885+71_3885+80del
XR_002957544.1:n.3999+71_3999+80del
XR_245681.4:n.3990+71_3990+80del
NM_001040108.2:c.3827+71_3827+80del MANE Select	NP_001035197.1:n.3827+71_3827+80del
NM_014381.3:c.3755+71_3755+80del	NP_055196.2:n.3755+71_3755+80del