Canonical Allele Identifier: CA2524737678

Gene: TOMT LRRC51 ANAPC15 LRTOMT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72109249_72109251del , CM000673.2:g.72109249_72109251del	GRCh38
NC_000011.9:g.71820295_71820297del , CM000673.1:g.71820295_71820297del	GRCh37
NC_000011.8:g.71497943_71497945del	NCBI36
NG_021423.1:g.33914_33916del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541899.3:c.*324_*326del (TOMT) MANE Select	ENSP00000494667.1:n.*324_*326del
ENST00000541899.2:c.*324_*326del (TOMT)	ENSP00000494667.1:n.*324_*326del
ENST00000307198.11:c.*324_*326del (LRRC51)	ENSP00000305742.7:n.*324_*326del
ENST00000419228.2:c.*611_*613del (LRRC51)	ENSP00000392233.2:n.*611_*613del
ENST00000427369.6:c.*919_*921del (LRRC51)	ENSP00000409403.2:n.*919_*921del
ENST00000435085.5:c.*324_*326del (LRRC51)	ENSP00000409789.1:n.*324_*326del
ENST00000502597.2:c.63+840_63+842del (ANAPC15)	ENSP00000441774.1:n.63+840_63+842del
ENST00000538117.5:c.*79_*81del (ANAPC15)	ENSP00000445212.1:n.*79_*81del
ENST00000543050.5:c.318+840_318+842del (ANAPC15)	ENSP00000437360.1:n.318+840_318+842del
ENST00000544409.5:c.*919_*921del (LRRC51)	ENSP00000440969.1:n.*919_*921del
NM_001145308.4:c.*324_*326del (LRTOMT)	NP_001138780.1:n.*324_*326del
NM_001145309.3:c.*324_*326del (LRTOMT)	NP_001138781.1:n.*324_*326del
NM_001145310.3:c.*324_*326del (LRTOMT)	NP_001138782.1:n.*324_*326del
XM_011544849.1:c.1425_1427del (LRTOMT)	XP_011543151.1:n.1425_1427del
NM_001330321.1:c.318+840_318+842del (ANAPC15)	NP_001317250.1:n.318+840_318+842del
XM_024448401.1:c.1425_1427del (LRTOMT)	XP_024304169.1:n.1425_1427del
NM_001145308.5:c.*324_*326del (LRTOMT)	NP_001138780.1:n.*324_*326del
NM_001145309.4:c.*324_*326del (LRTOMT)	NP_001138781.1:n.*324_*326del
NM_001145310.4:c.*324_*326del (LRTOMT)	NP_001138782.1:n.*324_*326del
NM_001330321.2:c.318+840_318+842del (ANAPC15)	NP_001317250.1:n.318+840_318+842del
NM_001393427.1:c.318+840_318+842del (ANAPC15)	NP_001380356.1:n.318+840_318+842del
NM_001393428.1:c.318+840_318+842del (ANAPC15)	NP_001380357.1:n.318+840_318+842del
NM_001393429.1:c.318+840_318+842del (ANAPC15)	NP_001380358.1:n.318+840_318+842del
NM_001393430.1:c.318+840_318+842del (ANAPC15)	NP_001380359.1:n.318+840_318+842del
NM_001393431.1:c.318+840_318+842del (ANAPC15)	NP_001380360.1:n.318+840_318+842del
NM_001393443.1:c.319-373_319-371del (ANAPC15)	NP_001380372.1:n.319-373_319-371del
NM_001393444.1:c.319-373_319-371del (ANAPC15)	NP_001380373.1:n.319-373_319-371del
NM_001393445.1:c.319-373_319-371del (ANAPC15)	NP_001380374.1:n.319-373_319-371del
NM_001393459.1:c.63+840_63+842del (ANAPC15)	NP_001380388.1:n.63+840_63+842del
NM_001393500.1:c.*324_*326del (TOMT)	NP_001380429.1:n.*324_*326del
NR_171687.1:n.548_550del (ANAPC15)
NM_001393500.2:c.*324_*326del (TOMT) MANE Select	NP_001380429.1:n.*324_*326del