Canonical Allele Identifier: CA2614916425

Gene: LRRC51 NUMA1 LRTOMT

Linked Data

• gnomAD v4: 11-72080591-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080591T>C , CM000673.2:g.72080591T>C	GRCh38
NC_000011.9:g.71791637T>C , CM000673.1:g.71791637T>C	GRCh37
NC_000011.8:g.71469285T>C	NCBI36
NG_021423.1:g.5256T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-434T>C (LRRC51)	ENSP00000289488.2:n.-434T>C
ENST00000535883.6:c.-311T>C (LRRC51)	ENSP00000437561.1:n.-311T>C
ENST00000538413.6:c.-350T>C (LRRC51)	ENSP00000438762.2:n.-350T>C
ENST00000642648.1:c.-311T>C (LRRC51)	ENSP00000494362.1:n.-311T>C
ENST00000642813.1:n.26T>C (LRRC51)
ENST00000307198.11:c.-616T>C (LRRC51)	ENSP00000305742.7:n.-616T>C
ENST00000393695.7:c.-236A>G (NUMA1)	ENSP00000377298.3:n.-236A>G
ENST00000535883.5:c.-434T>C (LRRC51)	ENSP00000437561.1:n.-434T>C
ENST00000538413.5:c.-311T>C (LRRC51)	ENSP00000438762.1:n.-311T>C
ENST00000543450.1:n.103A>G (NUMA1)
ENST00000613205.4:c.-236A>G (NUMA1)	ENSP00000480172.1:n.-236A>G
NM_001145307.4:c.-434T>C (LRTOMT)	NP_001138779.1:n.-434T>C
NM_001145308.4:c.-616T>C (LRTOMT)	NP_001138780.1:n.-616T>C
NM_001145309.3:c.-837T>C (LRTOMT)	NP_001138781.1:n.-837T>C
NM_001145310.3:c.-837T>C (LRTOMT)	NP_001138782.1:n.-837T>C
NM_001205138.3:c.-351T>C (LRTOMT)	NP_001192067.1:n.-351T>C
NM_001271471.2:c.-434T>C (LRTOMT)	NP_001258400.1:n.-434T>C
NM_001286561.1:c.-334A>G (NUMA1)	NP_001273490.1:n.-334A>G
NM_006185.3:c.-236A>G (NUMA1)	NP_006176.2:n.-236A>G
NM_145309.5:c.-434T>C (LRTOMT)	NP_660352.1:n.-434T>C
NR_026886.3:n.261T>C (LRTOMT)
XM_011545055.1:c.-236A>G (NUMA1)	XP_011543357.1:n.-236A>G
NM_001318803.1:c.-391T>C (LRTOMT)	NP_001305732.1:n.-391T>C
NR_134858.1:n.261T>C (LRTOMT)
XM_006718474.4:c.-350T>C (LRTOMT)	XP_006718537.1:n.-350T>C