Canonical Allele Identifier: CA2614916423

Gene: LRRC51 NUMA1 LRTOMT

Linked Data

• gnomAD v4: 11-72080590-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080590C>A , CM000673.2:g.72080590C>A	GRCh38
NC_000011.9:g.71791636C>A , CM000673.1:g.71791636C>A	GRCh37
NC_000011.8:g.71469284C>A	NCBI36
NG_021423.1:g.5255C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-435C>A (LRRC51)	ENSP00000289488.2:n.-435C>A
ENST00000535883.6:c.-312C>A (LRRC51)	ENSP00000437561.1:n.-312C>A
ENST00000538413.6:c.-351C>A (LRRC51)	ENSP00000438762.2:n.-351C>A
ENST00000642648.1:c.-312C>A (LRRC51)	ENSP00000494362.1:n.-312C>A
ENST00000642813.1:n.25C>A (LRRC51)
ENST00000307198.11:c.-617C>A (LRRC51)	ENSP00000305742.7:n.-617C>A
ENST00000393695.7:c.-235G>T (NUMA1)	ENSP00000377298.3:n.-235G>T
ENST00000535883.5:c.-435C>A (LRRC51)	ENSP00000437561.1:n.-435C>A
ENST00000538413.5:c.-312C>A (LRRC51)	ENSP00000438762.1:n.-312C>A
ENST00000543450.1:n.104G>T (NUMA1)
ENST00000613205.4:c.-235G>T (NUMA1)	ENSP00000480172.1:n.-235G>T
NM_001145307.4:c.-435C>A (LRTOMT)	NP_001138779.1:n.-435C>A
NM_001145308.4:c.-617C>A (LRTOMT)	NP_001138780.1:n.-617C>A
NM_001145309.3:c.-838C>A (LRTOMT)	NP_001138781.1:n.-838C>A
NM_001145310.3:c.-838C>A (LRTOMT)	NP_001138782.1:n.-838C>A
NM_001205138.3:c.-352C>A (LRTOMT)	NP_001192067.1:n.-352C>A
NM_001271471.2:c.-435C>A (LRTOMT)	NP_001258400.1:n.-435C>A
NM_001286561.1:c.-333G>T (NUMA1)	NP_001273490.1:n.-333G>T
NM_006185.3:c.-235G>T (NUMA1)	NP_006176.2:n.-235G>T
NM_145309.5:c.-435C>A (LRTOMT)	NP_660352.1:n.-435C>A
NR_026886.3:n.260C>A (LRTOMT)
XM_011545055.1:c.-235G>T (NUMA1)	XP_011543357.1:n.-235G>T
NM_001318803.1:c.-392C>A (LRTOMT)	NP_001305732.1:n.-392C>A
NR_134858.1:n.260C>A (LRTOMT)
XM_006718474.4:c.-351C>A (LRTOMT)	XP_006718537.1:n.-351C>A