Canonical Allele Identifier: CA2614916426

Gene: LRRC51 NUMA1 LRTOMT

Linked Data

• gnomAD v4: 11-72080592-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080592G>T , CM000673.2:g.72080592G>T	GRCh38
NC_000011.9:g.71791638G>T , CM000673.1:g.71791638G>T	GRCh37
NC_000011.8:g.71469286G>T	NCBI36
NG_021423.1:g.5257G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-433G>T (LRRC51)	ENSP00000289488.2:n.-433G>T
ENST00000535883.6:c.-310G>T (LRRC51)	ENSP00000437561.1:n.-310G>T
ENST00000538413.6:c.-349G>T (LRRC51)	ENSP00000438762.2:n.-349G>T
ENST00000642648.1:c.-310G>T (LRRC51)	ENSP00000494362.1:n.-310G>T
ENST00000642813.1:n.27G>T (LRRC51)
ENST00000307198.11:c.-615G>T (LRRC51)	ENSP00000305742.7:n.-615G>T
ENST00000393695.7:c.-237C>A (NUMA1)	ENSP00000377298.3:n.-237C>A
ENST00000535883.5:c.-433G>T (LRRC51)	ENSP00000437561.1:n.-433G>T
ENST00000538413.5:c.-310G>T (LRRC51)	ENSP00000438762.1:n.-310G>T
ENST00000543450.1:n.102C>A (NUMA1)
ENST00000613205.4:c.-237C>A (NUMA1)	ENSP00000480172.1:n.-237C>A
NM_001145307.4:c.-433G>T (LRTOMT)	NP_001138779.1:n.-433G>T
NM_001145308.4:c.-615G>T (LRTOMT)	NP_001138780.1:n.-615G>T
NM_001145309.3:c.-836G>T (LRTOMT)	NP_001138781.1:n.-836G>T
NM_001145310.3:c.-836G>T (LRTOMT)	NP_001138782.1:n.-836G>T
NM_001205138.3:c.-350G>T (LRTOMT)	NP_001192067.1:n.-350G>T
NM_001271471.2:c.-433G>T (LRTOMT)	NP_001258400.1:n.-433G>T
NM_001286561.1:c.-335C>A (NUMA1)	NP_001273490.1:n.-335C>A
NM_006185.3:c.-237C>A (NUMA1)	NP_006176.2:n.-237C>A
NM_145309.5:c.-433G>T (LRTOMT)	NP_660352.1:n.-433G>T
NR_026886.3:n.262G>T (LRTOMT)
XM_011545055.1:c.-237C>A (NUMA1)	XP_011543357.1:n.-237C>A
NM_001318803.1:c.-390G>T (LRTOMT)	NP_001305732.1:n.-390G>T
NR_134858.1:n.262G>T (LRTOMT)
XM_006718474.4:c.-349G>T (LRTOMT)	XP_006718537.1:n.-349G>T