Canonical Allele Identifier: CA1981839777

Gene: LRTOMT LRRC51

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72105798_72105799delinsCT , CM000673.2:g.72105798_72105799delinsCT	GRCh38
NC_000011.9:g.71816844_71816845delinsCT , CM000673.1:g.71816844_71816845delinsCT	GRCh37
NC_000011.8:g.71494492_71494493delinsCT	NCBI36
NG_021423.1:g.30463_30464delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643715.1:c.438-2807_438-2806delinsCT (LRTOMT)	ENSP00000496019.1:n.438-2807_438-2806delinsCT
ENST00000646163.1:c.73-258_73-257delinsCT (LRTOMT)	ENSP00000494749.1:n.73-258_73-257delinsCT
ENST00000307198.11:c.84-138_84-137delinsCT (LRRC51)	ENSP00000305742.7:n.84-138_84-137delinsCT
ENST00000419228.2:c.84-258_84-257delinsCT (LRRC51)	ENSP00000392233.2:n.84-258_84-257delinsCT
ENST00000427369.6:c.487-138_487-137delinsCT (LRRC51)	ENSP00000409403.2:n.487-138_487-137delinsCT
ENST00000435085.5:c.84-138_84-137delinsCT (LRRC51)	ENSP00000409789.1:n.84-138_84-137delinsCT
ENST00000439209.5:c.438-2807_438-2806delinsCT (LRRC51)	ENSP00000395139.1:n.438-2807_438-2806delinsCT
ENST00000541899.1:n.4_5delinsCT (LRRC51)
ENST00000544409.5:c.487-258_487-257delinsCT (LRRC51)	ENSP00000440969.1:n.487-258_487-257delinsCT
NM_001145308.4:c.84-138_84-137delinsCT (LRTOMT)	NP_001138780.1:n.84-138_84-137delinsCT
NM_001145309.3:c.84-138_84-137delinsCT (LRTOMT)	NP_001138781.1:n.84-138_84-137delinsCT
NM_001145310.3:c.84-258_84-257delinsCT (LRTOMT)	NP_001138782.1:n.84-258_84-257delinsCT
XM_011544849.1:c.309-138_309-137delinsCT (LRTOMT)	XP_011543151.1:n.309-138_309-137delinsCT
XM_024448401.1:c.309-138_309-137delinsCT (LRTOMT)	XP_024304169.1:n.309-138_309-137delinsCT
NM_001145308.5:c.84-138_84-137delinsCT (LRTOMT)	NP_001138780.1:n.84-138_84-137delinsCT
NM_001145309.4:c.84-138_84-137delinsCT (LRTOMT)	NP_001138781.1:n.84-138_84-137delinsCT
NM_001145310.4:c.84-258_84-257delinsCT (LRTOMT)	NP_001138782.1:n.84-258_84-257delinsCT