Canonical Allele Identifier: CA1981828432

Gene: LRRC51 NUMA1 LRTOMT

Linked Data

• dbSNP Id: rs1591116635

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080639A>C , CM000673.2:g.72080639A>C	GRCh38
NC_000011.9:g.71791685A>C , CM000673.1:g.71791685A>C	GRCh37
NC_000011.8:g.71469333A>C	NCBI36
NG_021423.1:g.5304A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-386A>C (LRRC51)	ENSP00000289488.2:n.-386A>C
ENST00000535883.6:c.-263A>C (LRRC51)	ENSP00000437561.1:n.-263A>C
ENST00000538413.6:c.-302A>C (LRRC51)	ENSP00000438762.2:n.-302A>C
ENST00000539271.6:c.-456A>C (LRRC51)	ENSP00000442267.2:n.-456A>C
ENST00000642648.1:c.-263A>C (LRRC51)	ENSP00000494362.1:n.-263A>C
ENST00000642813.1:n.74A>C (LRRC51)
ENST00000647530.1:c.-549A>C (LRRC51)	ENSP00000494072.1:n.-549A>C
ENST00000307198.11:c.-568A>C (LRRC51)	ENSP00000305742.7:n.-568A>C
ENST00000393695.7:c.-284T>G (NUMA1)	ENSP00000377298.3:n.-284T>G
ENST00000535883.5:c.-386A>C (LRRC51)	ENSP00000437561.1:n.-386A>C
ENST00000538413.5:c.-263A>C (LRRC51)	ENSP00000438762.1:n.-263A>C
ENST00000543450.1:n.55T>G (NUMA1)
ENST00000613205.4:c.-284T>G (NUMA1)	ENSP00000480172.1:n.-284T>G
NM_001145307.4:c.-386A>C (LRTOMT)	NP_001138779.1:n.-386A>C
NM_001145308.4:c.-568A>C (LRTOMT)	NP_001138780.1:n.-568A>C
NM_001145309.3:c.-789A>C (LRTOMT)	NP_001138781.1:n.-789A>C
NM_001145310.3:c.-789A>C (LRTOMT)	NP_001138782.1:n.-789A>C
NM_001205138.3:c.-303A>C (LRTOMT)	NP_001192067.1:n.-303A>C
NM_001271471.2:c.-386A>C (LRTOMT)	NP_001258400.1:n.-386A>C
NM_001286561.1:c.-382T>G (NUMA1)	NP_001273490.1:n.-382T>G
NM_006185.3:c.-284T>G (NUMA1)	NP_006176.2:n.-284T>G
NM_145309.5:c.-386A>C (LRTOMT)	NP_660352.1:n.-386A>C
NR_026886.3:n.309A>C (LRTOMT)
XM_011545055.1:c.-284T>G (NUMA1)	XP_011543357.1:n.-284T>G
NM_001318803.1:c.-343A>C (LRTOMT)	NP_001305732.1:n.-343A>C
NR_134858.1:n.309A>C (LRTOMT)
XM_006718474.4:c.-302A>C (LRTOMT)	XP_006718537.1:n.-302A>C
XM_011544848.3:c.-549A>C (LRTOMT)	XP_011543150.1:n.-549A>C