Canonical Allele Identifier: CA1981828492

Gene: LRRC51 LRTOMT

Linked Data

• dbSNP Id: rs1944106598

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080750A>G , CM000673.2:g.72080750A>G	GRCh38
NC_000011.9:g.71791796A>G , CM000673.1:g.71791796A>G	GRCh37
NC_000011.8:g.71469444A>G	NCBI36
NG_021423.1:g.5415A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-275A>G (LRRC51)	ENSP00000289488.2:n.-275A>G
ENST00000535883.6:c.-152A>G (LRRC51)	ENSP00000437561.1:n.-152A>G
ENST00000538413.6:c.-191A>G (LRRC51)	ENSP00000438762.2:n.-191A>G
ENST00000539271.6:c.-345A>G (LRRC51)	ENSP00000442267.2:n.-345A>G
ENST00000642510.1:c.-468A>G (LRRC51)	ENSP00000496544.1:n.-468A>G
ENST00000642648.1:c.-152A>G (LRRC51)	ENSP00000494362.1:n.-152A>G
ENST00000642813.1:n.185A>G (LRRC51)
ENST00000647530.1:c.-438A>G (LRRC51)	ENSP00000494072.1:n.-438A>G
ENST00000289488.6:c.-275A>G (LRRC51)	ENSP00000289488.2:n.-275A>G
ENST00000307198.11:c.-457A>G (LRRC51)	ENSP00000305742.7:n.-457A>G
ENST00000535883.5:c.-275A>G (LRRC51)	ENSP00000437561.1:n.-275A>G
ENST00000538413.5:c.-152A>G (LRRC51)	ENSP00000438762.1:n.-152A>G
NM_001145307.4:c.-275A>G (LRTOMT)	NP_001138779.1:n.-275A>G
NM_001145308.4:c.-457A>G (LRTOMT)	NP_001138780.1:n.-457A>G
NM_001145309.3:c.-678A>G (LRTOMT)	NP_001138781.1:n.-678A>G
NM_001145310.3:c.-678A>G (LRTOMT)	NP_001138782.1:n.-678A>G
NM_001205138.3:c.-192A>G (LRTOMT)	NP_001192067.1:n.-192A>G
NM_001271471.2:c.-275A>G (LRTOMT)	NP_001258400.1:n.-275A>G
NM_145309.5:c.-275A>G (LRTOMT)	NP_660352.1:n.-275A>G
NR_026886.3:n.420A>G (LRTOMT)
XM_006718473.2:c.-152A>G (LRTOMT)	XP_006718536.1:n.-152A>G
NM_001318803.1:c.-232A>G (LRTOMT)	NP_001305732.1:n.-232A>G
NR_134858.1:n.420A>G (LRTOMT)
XM_006718473.4:c.-152A>G (LRTOMT)	XP_006718536.1:n.-152A>G
XM_006718474.4:c.-191A>G (LRTOMT)	XP_006718537.1:n.-191A>G
XM_011544848.3:c.-438A>G (LRTOMT)	XP_011543150.1:n.-438A>G