Canonical Allele Identifier: CA1981841225

Gene: TOMT LRRC51 ANAPC15 LRTOMT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72109041_72109043delinsGGA , CM000673.2:g.72109041_72109043delinsGGA	GRCh38
NC_000011.9:g.71820087_71820089delinsGGA , CM000673.1:g.71820087_71820089delinsGGA	GRCh37
NC_000011.8:g.71497735_71497737delinsGGA	NCBI36
NG_021423.1:g.33706_33708delinsGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541899.3:c.*116_*118delinsGGA (TOMT) MANE Select	ENSP00000494667.1:n.*116_*118delinsGGA
ENST00000541899.2:c.*116_*118delinsGGA (TOMT)	ENSP00000494667.1:n.*116_*118delinsGGA
ENST00000307198.11:c.*116_*118delinsGGA (LRRC51)	ENSP00000305742.7:n.*116_*118delinsGGA
ENST00000419228.2:c.*403_*405delinsGGA (LRRC51)	ENSP00000392233.2:n.*403_*405delinsGGA
ENST00000427369.6:c.*711_*713delinsGGA (LRRC51)	ENSP00000409403.2:n.*711_*713delinsGGA
ENST00000435085.5:c.*116_*118delinsGGA (LRRC51)	ENSP00000409789.1:n.*116_*118delinsGGA
ENST00000502597.2:c.63+1045_63+1047delinsTCC (ANAPC15)	ENSP00000441774.1:n.63+1045_63+1047delinsTCC
ENST00000538117.5:c.*99-168_*99-166delinsTCC (ANAPC15)	ENSP00000445212.1:n.*99-168_*99-166delinsTCC
ENST00000543050.5:c.318+1045_318+1047delinsTCC (ANAPC15)	ENSP00000437360.1:n.318+1045_318+1047delinsTCC
ENST00000544409.5:c.*711_*713delinsGGA (LRRC51)	ENSP00000440969.1:n.*711_*713delinsGGA
NM_001145308.4:c.*116_*118delinsGGA (LRTOMT)	NP_001138780.1:n.*116_*118delinsGGA
NM_001145309.3:c.*116_*118delinsGGA (LRTOMT)	NP_001138781.1:n.*116_*118delinsGGA
NM_001145310.3:c.*116_*118delinsGGA (LRTOMT)	NP_001138782.1:n.*116_*118delinsGGA
XM_011544849.1:c.1217_1219delinsGGA (LRTOMT)	XP_011543151.1:n.1217_1219delinsGGA
NM_001330321.1:c.318+1045_318+1047delinsTCC (ANAPC15)	NP_001317250.1:n.318+1045_318+1047delinsTCC
XM_024448401.1:c.1217_1219delinsGGA (LRTOMT)	XP_024304169.1:n.1217_1219delinsGGA
NM_001145308.5:c.*116_*118delinsGGA (LRTOMT)	NP_001138780.1:n.*116_*118delinsGGA
NM_001145309.4:c.*116_*118delinsGGA (LRTOMT)	NP_001138781.1:n.*116_*118delinsGGA
NM_001145310.4:c.*116_*118delinsGGA (LRTOMT)	NP_001138782.1:n.*116_*118delinsGGA
NM_001330321.2:c.318+1045_318+1047delinsTCC (ANAPC15)	NP_001317250.1:n.318+1045_318+1047delinsTCC
NM_001393427.1:c.318+1045_318+1047delinsTCC (ANAPC15)	NP_001380356.1:n.318+1045_318+1047delinsTCC
NM_001393428.1:c.318+1045_318+1047delinsTCC (ANAPC15)	NP_001380357.1:n.318+1045_318+1047delinsTCC
NM_001393429.1:c.318+1045_318+1047delinsTCC (ANAPC15)	NP_001380358.1:n.318+1045_318+1047delinsTCC
NM_001393430.1:c.318+1045_318+1047delinsTCC (ANAPC15)	NP_001380359.1:n.318+1045_318+1047delinsTCC
NM_001393431.1:c.318+1045_318+1047delinsTCC (ANAPC15)	NP_001380360.1:n.318+1045_318+1047delinsTCC
NM_001393443.1:c.319-168_319-166delinsTCC (ANAPC15)	NP_001380372.1:n.319-168_319-166delinsTCC
NM_001393444.1:c.319-168_319-166delinsTCC (ANAPC15)	NP_001380373.1:n.319-168_319-166delinsTCC
NM_001393445.1:c.319-168_319-166delinsTCC (ANAPC15)	NP_001380374.1:n.319-168_319-166delinsTCC
NM_001393459.1:c.63+1045_63+1047delinsTCC (ANAPC15)	NP_001380388.1:n.63+1045_63+1047delinsTCC
NM_001393500.1:c.*116_*118delinsGGA (TOMT)	NP_001380429.1:n.*116_*118delinsGGA
NR_171687.1:n.568-168_568-166delinsTCC (ANAPC15)
NM_001393500.2:c.*116_*118delinsGGA (TOMT) MANE Select	NP_001380429.1:n.*116_*118delinsGGA