Canonical Allele Identifier: CA1981839902

Gene: TOMT LRTOMT LRRC51

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72106082G= , CM000673.2:g.72106082G=	GRCh38
NC_000011.9:g.71817128G= , CM000673.1:g.71817128G=	GRCh37
NC_000011.8:g.71494776G=	NCBI36
NG_021423.1:g.30747G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541899.3:c.131G= (TOMT) MANE Select	ENSP00000494667.1:p.Arg44=
ENST00000541899.2:c.131G= (TOMT)	ENSP00000494667.1:p.Arg44=
ENST00000643715.1:c.438-2523G= (LRTOMT)	ENSP00000496019.1:n.438-2523G=
ENST00000646163.1:c.99G= (LRTOMT)	ENSP00000494749.1:p.Ala33=
ENST00000307198.11:c.230G= (LRRC51)	ENSP00000305742.7:p.Arg77=
ENST00000419228.2:c.110G= (LRRC51)	ENSP00000392233.2:p.Arg37=
ENST00000427369.6:c.633G= (LRRC51)	ENSP00000409403.2:p.Ala211=
ENST00000435085.5:c.230G= (LRRC51)	ENSP00000409789.1:p.Arg77=
ENST00000439209.5:c.438-2523G= (LRRC51)	ENSP00000395139.1:n.438-2523G=
ENST00000541899.1:n.288G= (LRRC51)
ENST00000544409.5:c.513G= (LRRC51)	ENSP00000440969.1:p.Ala171=
NM_001145308.4:c.230G= (LRTOMT)	NP_001138780.1:p.Arg77=
NM_001145309.3:c.230G= (LRTOMT)	NP_001138781.1:p.Arg77=
NM_001145310.3:c.110G= (LRTOMT)	NP_001138782.1:p.Arg37=
XM_011544849.1:c.455G= (LRTOMT)	XP_011543151.1:p.Arg152=
XM_024448401.1:c.455G= (LRTOMT)	XP_024304169.1:p.Arg152=
NM_001145308.5:c.230G= (LRTOMT)	NP_001138780.1:p.Arg77=
NM_001145309.4:c.230G= (LRTOMT)	NP_001138781.1:p.Arg77=
NM_001145310.4:c.110G= (LRTOMT)	NP_001138782.1:p.Arg37=
NM_001393500.1:c.131G= (TOMT)	NP_001380429.1:p.Arg44=
NM_001393500.2:c.131G= (TOMT) MANE Select	NP_001380429.1:p.Arg44=