Canonical Allele Identifier: CA1981828446

Gene: LRRC51 NUMA1 LRTOMT

Linked Data

• dbSNP Id: rs951073046

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080659T>G , CM000673.2:g.72080659T>G	GRCh38
NC_000011.9:g.71791705T>G , CM000673.1:g.71791705T>G	GRCh37
NC_000011.8:g.71469353T>G	NCBI36
NG_021423.1:g.5324T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-366T>G (LRRC51)	ENSP00000289488.2:n.-366T>G
ENST00000535883.6:c.-243T>G (LRRC51)	ENSP00000437561.1:n.-243T>G
ENST00000538413.6:c.-282T>G (LRRC51)	ENSP00000438762.2:n.-282T>G
ENST00000539271.6:c.-436T>G (LRRC51)	ENSP00000442267.2:n.-436T>G
ENST00000642648.1:c.-243T>G (LRRC51)	ENSP00000494362.1:n.-243T>G
ENST00000642813.1:n.94T>G (LRRC51)
ENST00000647530.1:c.-529T>G (LRRC51)	ENSP00000494072.1:n.-529T>G
ENST00000289488.6:c.-366T>G (LRRC51)	ENSP00000289488.2:n.-366T>G
ENST00000307198.11:c.-548T>G (LRRC51)	ENSP00000305742.7:n.-548T>G
ENST00000393695.7:c.-304A>C (NUMA1)	ENSP00000377298.3:n.-304A>C
ENST00000535883.5:c.-366T>G (LRRC51)	ENSP00000437561.1:n.-366T>G
ENST00000538413.5:c.-243T>G (LRRC51)	ENSP00000438762.1:n.-243T>G
ENST00000543450.1:n.35A>C (NUMA1)
ENST00000613205.4:c.-304A>C (NUMA1)	ENSP00000480172.1:n.-304A>C
NM_001145307.4:c.-366T>G (LRTOMT)	NP_001138779.1:n.-366T>G
NM_001145308.4:c.-548T>G (LRTOMT)	NP_001138780.1:n.-548T>G
NM_001145309.3:c.-769T>G (LRTOMT)	NP_001138781.1:n.-769T>G
NM_001145310.3:c.-769T>G (LRTOMT)	NP_001138782.1:n.-769T>G
NM_001205138.3:c.-283T>G (LRTOMT)	NP_001192067.1:n.-283T>G
NM_001271471.2:c.-366T>G (LRTOMT)	NP_001258400.1:n.-366T>G
NM_001286561.1:c.-402A>C (NUMA1)	NP_001273490.1:n.-402A>C
NM_006185.3:c.-304A>C (NUMA1)	NP_006176.2:n.-304A>C
NM_145309.5:c.-366T>G (LRTOMT)	NP_660352.1:n.-366T>G
NR_026886.3:n.329T>G (LRTOMT)
XM_011545055.1:c.-304A>C (NUMA1)	XP_011543357.1:n.-304A>C
NM_001318803.1:c.-323T>G (LRTOMT)	NP_001305732.1:n.-323T>G
NR_134858.1:n.329T>G (LRTOMT)
XM_006718474.4:c.-282T>G (LRTOMT)	XP_006718537.1:n.-282T>G
XM_011544848.3:c.-529T>G (LRTOMT)	XP_011543150.1:n.-529T>G