Canonical Allele Identifier: CA939427115

Gene: LRRC51 NUMA1 LRTOMT

Linked Data

• dbSNP Id: rs1944097350
• gnomAD v3: 11-72080638-C-T
• gnomAD v4: 11-72080638-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080638C>T , CM000673.2:g.72080638C>T	GRCh38
NC_000011.9:g.71791684C>T , CM000673.1:g.71791684C>T	GRCh37
NC_000011.8:g.71469332C>T	NCBI36
NG_021423.1:g.5303C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-387C>T (LRRC51)	ENSP00000289488.2:n.-387C>T
ENST00000535883.6:c.-264C>T (LRRC51)	ENSP00000437561.1:n.-264C>T
ENST00000538413.6:c.-303C>T (LRRC51)	ENSP00000438762.2:n.-303C>T
ENST00000539271.6:c.-457C>T (LRRC51)	ENSP00000442267.2:n.-457C>T
ENST00000642648.1:c.-264C>T (LRRC51)	ENSP00000494362.1:n.-264C>T
ENST00000642813.1:n.73C>T (LRRC51)
ENST00000647530.1:c.-550C>T (LRRC51)	ENSP00000494072.1:n.-550C>T
ENST00000307198.11:c.-569C>T (LRRC51)	ENSP00000305742.7:n.-569C>T
ENST00000393695.7:c.-283G>A (NUMA1)	ENSP00000377298.3:n.-283G>A
ENST00000535883.5:c.-387C>T (LRRC51)	ENSP00000437561.1:n.-387C>T
ENST00000538413.5:c.-264C>T (LRRC51)	ENSP00000438762.1:n.-264C>T
ENST00000543450.1:n.56G>A (NUMA1)
ENST00000613205.4:c.-283G>A (NUMA1)	ENSP00000480172.1:n.-283G>A
NM_001145307.4:c.-387C>T (LRTOMT)	NP_001138779.1:n.-387C>T
NM_001145308.4:c.-569C>T (LRTOMT)	NP_001138780.1:n.-569C>T
NM_001145309.3:c.-790C>T (LRTOMT)	NP_001138781.1:n.-790C>T
NM_001145310.3:c.-790C>T (LRTOMT)	NP_001138782.1:n.-790C>T
NM_001205138.3:c.-304C>T (LRTOMT)	NP_001192067.1:n.-304C>T
NM_001271471.2:c.-387C>T (LRTOMT)	NP_001258400.1:n.-387C>T
NM_001286561.1:c.-381G>A (NUMA1)	NP_001273490.1:n.-381G>A
NM_006185.3:c.-283G>A (NUMA1)	NP_006176.2:n.-283G>A
NM_145309.5:c.-387C>T (LRTOMT)	NP_660352.1:n.-387C>T
NR_026886.3:n.308C>T (LRTOMT)
XM_011545055.1:c.-283G>A (NUMA1)	XP_011543357.1:n.-283G>A
NM_001318803.1:c.-344C>T (LRTOMT)	NP_001305732.1:n.-344C>T
NR_134858.1:n.308C>T (LRTOMT)
XM_006718474.4:c.-303C>T (LRTOMT)	XP_006718537.1:n.-303C>T
XM_011544848.3:c.-550C>T (LRTOMT)	XP_011543150.1:n.-550C>T