Canonical Allele Identifier: CA1981828481

Gene: LRRC51 LRTOMT

Linked Data

• dbSNP Id: rs1944105413

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080720C>A , CM000673.2:g.72080720C>A	GRCh38
NC_000011.9:g.71791766C>A , CM000673.1:g.71791766C>A	GRCh37
NC_000011.8:g.71469414C>A	NCBI36
NG_021423.1:g.5385C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-305C>A (LRRC51)	ENSP00000289488.2:n.-305C>A
ENST00000535883.6:c.-182C>A (LRRC51)	ENSP00000437561.1:n.-182C>A
ENST00000538413.6:c.-221C>A (LRRC51)	ENSP00000438762.2:n.-221C>A
ENST00000539271.6:c.-375C>A (LRRC51)	ENSP00000442267.2:n.-375C>A
ENST00000642510.1:c.-498C>A (LRRC51)	ENSP00000496544.1:n.-498C>A
ENST00000642648.1:c.-182C>A (LRRC51)	ENSP00000494362.1:n.-182C>A
ENST00000642813.1:n.155C>A (LRRC51)
ENST00000647530.1:c.-468C>A (LRRC51)	ENSP00000494072.1:n.-468C>A
ENST00000289488.6:c.-305C>A (LRRC51)	ENSP00000289488.2:n.-305C>A
ENST00000307198.11:c.-487C>A (LRRC51)	ENSP00000305742.7:n.-487C>A
ENST00000535883.5:c.-305C>A (LRRC51)	ENSP00000437561.1:n.-305C>A
ENST00000538413.5:c.-182C>A (LRRC51)	ENSP00000438762.1:n.-182C>A
NM_001145307.4:c.-305C>A (LRTOMT)	NP_001138779.1:n.-305C>A
NM_001145308.4:c.-487C>A (LRTOMT)	NP_001138780.1:n.-487C>A
NM_001145309.3:c.-708C>A (LRTOMT)	NP_001138781.1:n.-708C>A
NM_001145310.3:c.-708C>A (LRTOMT)	NP_001138782.1:n.-708C>A
NM_001205138.3:c.-222C>A (LRTOMT)	NP_001192067.1:n.-222C>A
NM_001271471.2:c.-305C>A (LRTOMT)	NP_001258400.1:n.-305C>A
NM_145309.5:c.-305C>A (LRTOMT)	NP_660352.1:n.-305C>A
NR_026886.3:n.390C>A (LRTOMT)
XM_006718473.2:c.-182C>A (LRTOMT)	XP_006718536.1:n.-182C>A
NM_001318803.1:c.-262C>A (LRTOMT)	NP_001305732.1:n.-262C>A
NR_134858.1:n.390C>A (LRTOMT)
XM_006718473.4:c.-182C>A (LRTOMT)	XP_006718536.1:n.-182C>A
XM_006718474.4:c.-221C>A (LRTOMT)	XP_006718537.1:n.-221C>A
XM_011544848.3:c.-468C>A (LRTOMT)	XP_011543150.1:n.-468C>A