Canonical Allele Identifier: CA224380534

Gene: LRRC51 NUMA1 LRTOMT

Linked Data

• dbSNP Id: rs972621478
• gnomAD v2: 11-71791640-CG-C
• gnomAD v3: 11-72080594-CG-C
• gnomAD v4: 11-72080594-CG-C
• MyVariant Identifiers: chr11:g.71791641del (hg19) ; chr11:g.72080595del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080596del , CM000673.2:g.72080596del	GRCh38
NC_000011.9:g.71791642del , CM000673.1:g.71791642del	GRCh37
NC_000011.8:g.71469290del	NCBI36
NG_021423.1:g.5261del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-429del (LRRC51)	ENSP00000289488.2:n.-429del
ENST00000535883.6:c.-306del (LRRC51)	ENSP00000437561.1:n.-306del
ENST00000538413.6:c.-345del (LRRC51)	ENSP00000438762.2:n.-345del
ENST00000642648.1:c.-306del (LRRC51)	ENSP00000494362.1:n.-306del
ENST00000642813.1:n.31del (LRRC51)
ENST00000647530.1:c.-592del (LRRC51)	ENSP00000494072.1:n.-592del
ENST00000307198.11:c.-611del (LRRC51)	ENSP00000305742.7:n.-611del
ENST00000393695.7:c.-240del (NUMA1)	ENSP00000377298.3:n.-240del
ENST00000535883.5:c.-429del (LRRC51)	ENSP00000437561.1:n.-429del
ENST00000538413.5:c.-306del (LRRC51)	ENSP00000438762.1:n.-306del
ENST00000543450.1:n.99del (NUMA1)
ENST00000613205.4:c.-240del (NUMA1)	ENSP00000480172.1:n.-240del
NM_001145307.4:c.-429del (LRTOMT)	NP_001138779.1:n.-429del
NM_001145308.4:c.-611del (LRTOMT)	NP_001138780.1:n.-611del
NM_001145309.3:c.-832del (LRTOMT)	NP_001138781.1:n.-832del
NM_001145310.3:c.-832del (LRTOMT)	NP_001138782.1:n.-832del
NM_001205138.3:c.-346del (LRTOMT)	NP_001192067.1:n.-346del
NM_001271471.2:c.-429del (LRTOMT)	NP_001258400.1:n.-429del
NM_001286561.1:c.-338del (NUMA1)	NP_001273490.1:n.-338del
NM_006185.3:c.-240del (NUMA1)	NP_006176.2:n.-240del
NM_145309.5:c.-429del (LRTOMT)	NP_660352.1:n.-429del
NR_026886.3:n.266del (LRTOMT)
XM_011545055.1:c.-240del (NUMA1)	XP_011543357.1:n.-240del
NM_001318803.1:c.-386del (LRTOMT)	NP_001305732.1:n.-386del
NR_134858.1:n.266del (LRTOMT)
XM_006718474.4:c.-345del (LRTOMT)	XP_006718537.1:n.-345del