Canonical Allele Identifier: CA224380550

Gene: LRRC51 NUMA1 LRTOMT

Linked Data

• dbSNP Id: rs982303614
• gnomAD v3: 11-72080625-G-C
• gnomAD v4: 11-72080625-G-C
• MyVariant Identifiers: chr11:g.71791671G>C (hg19) ; chr11:g.72080625G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080625G>C , CM000673.2:g.72080625G>C	GRCh38
NC_000011.9:g.71791671G>C , CM000673.1:g.71791671G>C	GRCh37
NC_000011.8:g.71469319G>C	NCBI36
NG_021423.1:g.5290G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-400G>C (LRRC51)	ENSP00000289488.2:n.-400G>C
ENST00000535883.6:c.-277G>C (LRRC51)	ENSP00000437561.1:n.-277G>C
ENST00000538413.6:c.-316G>C (LRRC51)	ENSP00000438762.2:n.-316G>C
ENST00000539271.6:c.-470G>C (LRRC51)	ENSP00000442267.2:n.-470G>C
ENST00000642648.1:c.-277G>C (LRRC51)	ENSP00000494362.1:n.-277G>C
ENST00000642813.1:n.60G>C (LRRC51)
ENST00000647530.1:c.-563G>C (LRRC51)	ENSP00000494072.1:n.-563G>C
ENST00000307198.11:c.-582G>C (LRRC51)	ENSP00000305742.7:n.-582G>C
ENST00000393695.7:c.-270C>G (NUMA1)	ENSP00000377298.3:n.-270C>G
ENST00000535883.5:c.-400G>C (LRRC51)	ENSP00000437561.1:n.-400G>C
ENST00000538413.5:c.-277G>C (LRRC51)	ENSP00000438762.1:n.-277G>C
ENST00000543450.1:n.69C>G (NUMA1)
ENST00000613205.4:c.-270C>G (NUMA1)	ENSP00000480172.1:n.-270C>G
NM_001145307.4:c.-400G>C (LRTOMT)	NP_001138779.1:n.-400G>C
NM_001145308.4:c.-582G>C (LRTOMT)	NP_001138780.1:n.-582G>C
NM_001145309.3:c.-803G>C (LRTOMT)	NP_001138781.1:n.-803G>C
NM_001145310.3:c.-803G>C (LRTOMT)	NP_001138782.1:n.-803G>C
NM_001205138.3:c.-317G>C (LRTOMT)	NP_001192067.1:n.-317G>C
NM_001271471.2:c.-400G>C (LRTOMT)	NP_001258400.1:n.-400G>C
NM_001286561.1:c.-368C>G (NUMA1)	NP_001273490.1:n.-368C>G
NM_006185.3:c.-270C>G (NUMA1)	NP_006176.2:n.-270C>G
NM_145309.5:c.-400G>C (LRTOMT)	NP_660352.1:n.-400G>C
NR_026886.3:n.295G>C (LRTOMT)
XM_011545055.1:c.-270C>G (NUMA1)	XP_011543357.1:n.-270C>G
NM_001318803.1:c.-357G>C (LRTOMT)	NP_001305732.1:n.-357G>C
NR_134858.1:n.295G>C (LRTOMT)
XM_006718474.4:c.-316G>C (LRTOMT)	XP_006718537.1:n.-316G>C
XM_011544848.3:c.-563G>C (LRTOMT)	XP_011543150.1:n.-563G>C