Canonical Allele Identifier: CA381716362

Gene: LRTOMT LRRC51

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72104984C>A , CM000673.2:g.72104984C>A	GRCh38
NC_000011.9:g.71816030C>A , CM000673.1:g.71816030C>A	GRCh37
NC_000011.8:g.71493678C>A	NCBI36
NG_021423.1:g.29649C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643715.1:c.438-3621C>A (LRTOMT)	ENSP00000496019.1:n.438-3621C>A
ENST00000646163.1:c.44C>A (LRTOMT)	ENSP00000494749.1:p.Pro15His
ENST00000307198.11:c.55C>A (LRRC51)	ENSP00000305742.7:p.Leu19Met
ENST00000419228.2:c.55C>A (LRRC51)	ENSP00000392233.2:p.Leu19Met
ENST00000427369.6:c.458C>A (LRRC51)	ENSP00000409403.2:p.Pro153His
ENST00000435085.5:c.55C>A (LRRC51)	ENSP00000409789.1:p.Leu19Met
ENST00000439209.5:c.438-3621C>A (LRRC51)	ENSP00000395139.1:n.438-3621C>A
ENST00000544409.5:c.458C>A (LRRC51)	ENSP00000440969.1:p.Pro153His
NM_001145308.4:c.55C>A (LRTOMT)	NP_001138780.1:p.Leu19Met
NM_001145309.3:c.55C>A (LRTOMT)	NP_001138781.1:p.Leu19Met
NM_001145310.3:c.55C>A (LRTOMT)	NP_001138782.1:p.Leu19Met
XM_011544849.1:c.280C>A (LRTOMT)	XP_011543151.1:p.Leu94Met
XM_024448401.1:c.280C>A (LRTOMT)	XP_024304169.1:p.Leu94Met
NM_001145308.5:c.55C>A (LRTOMT)	NP_001138780.1:p.Leu19Met
NM_001145309.4:c.55C>A (LRTOMT)	NP_001138781.1:p.Leu19Met
NM_001145310.4:c.55C>A (LRTOMT)	NP_001138782.1:p.Leu19Met