Canonical Allele Identifier: CA1981828477

Gene: LRRC51 LRTOMT

Linked Data

• dbSNP Id: rs1565308725

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080717T>A , CM000673.2:g.72080717T>A	GRCh38
NC_000011.9:g.71791763T>A , CM000673.1:g.71791763T>A	GRCh37
NC_000011.8:g.71469411T>A	NCBI36
NG_021423.1:g.5382T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-308T>A (LRRC51)	ENSP00000289488.2:n.-308T>A
ENST00000535883.6:c.-185T>A (LRRC51)	ENSP00000437561.1:n.-185T>A
ENST00000538413.6:c.-224T>A (LRRC51)	ENSP00000438762.2:n.-224T>A
ENST00000539271.6:c.-378T>A (LRRC51)	ENSP00000442267.2:n.-378T>A
ENST00000642510.1:c.-501T>A (LRRC51)	ENSP00000496544.1:n.-501T>A
ENST00000642648.1:c.-185T>A (LRRC51)	ENSP00000494362.1:n.-185T>A
ENST00000642813.1:n.152T>A (LRRC51)
ENST00000647530.1:c.-471T>A (LRRC51)	ENSP00000494072.1:n.-471T>A
ENST00000289488.6:c.-308T>A (LRRC51)	ENSP00000289488.2:n.-308T>A
ENST00000307198.11:c.-490T>A (LRRC51)	ENSP00000305742.7:n.-490T>A
ENST00000535883.5:c.-308T>A (LRRC51)	ENSP00000437561.1:n.-308T>A
ENST00000538413.5:c.-185T>A (LRRC51)	ENSP00000438762.1:n.-185T>A
NM_001145307.4:c.-308T>A (LRTOMT)	NP_001138779.1:n.-308T>A
NM_001145308.4:c.-490T>A (LRTOMT)	NP_001138780.1:n.-490T>A
NM_001145309.3:c.-711T>A (LRTOMT)	NP_001138781.1:n.-711T>A
NM_001145310.3:c.-711T>A (LRTOMT)	NP_001138782.1:n.-711T>A
NM_001205138.3:c.-225T>A (LRTOMT)	NP_001192067.1:n.-225T>A
NM_001271471.2:c.-308T>A (LRTOMT)	NP_001258400.1:n.-308T>A
NM_145309.5:c.-308T>A (LRTOMT)	NP_660352.1:n.-308T>A
NR_026886.3:n.387T>A (LRTOMT)
XM_006718473.2:c.-185T>A (LRTOMT)	XP_006718536.1:n.-185T>A
NM_001318803.1:c.-265T>A (LRTOMT)	NP_001305732.1:n.-265T>A
NR_134858.1:n.387T>A (LRTOMT)
XM_006718473.4:c.-185T>A (LRTOMT)	XP_006718536.1:n.-185T>A
XM_006718474.4:c.-224T>A (LRTOMT)	XP_006718537.1:n.-224T>A
XM_011544848.3:c.-471T>A (LRTOMT)	XP_011543150.1:n.-471T>A