Canonical Allele Identifier: CA679952730

Gene: LRRC51 NUMA1 LRTOMT

Linked Data

• dbSNP Id: rs1228038021
• gnomAD v4: 11-72080595-G-A
• MyVariant Identifiers: chr11:g.71791641G>A (hg19) ; chr11:g.72080595G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080595G>A , CM000673.2:g.72080595G>A	GRCh38
NC_000011.9:g.71791641G>A , CM000673.1:g.71791641G>A	GRCh37
NC_000011.8:g.71469289G>A	NCBI36
NG_021423.1:g.5260G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-430G>A (LRRC51)	ENSP00000289488.2:n.-430G>A
ENST00000535883.6:c.-307G>A (LRRC51)	ENSP00000437561.1:n.-307G>A
ENST00000538413.6:c.-346G>A (LRRC51)	ENSP00000438762.2:n.-346G>A
ENST00000642648.1:c.-307G>A (LRRC51)	ENSP00000494362.1:n.-307G>A
ENST00000642813.1:n.30G>A (LRRC51)
ENST00000647530.1:c.-593G>A (LRRC51)	ENSP00000494072.1:n.-593G>A
ENST00000307198.11:c.-612G>A (LRRC51)	ENSP00000305742.7:n.-612G>A
ENST00000393695.7:c.-240C>T (NUMA1)	ENSP00000377298.3:n.-240C>T
ENST00000535883.5:c.-430G>A (LRRC51)	ENSP00000437561.1:n.-430G>A
ENST00000538413.5:c.-307G>A (LRRC51)	ENSP00000438762.1:n.-307G>A
ENST00000543450.1:n.99C>T (NUMA1)
ENST00000613205.4:c.-240C>T (NUMA1)	ENSP00000480172.1:n.-240C>T
NM_001145307.4:c.-430G>A (LRTOMT)	NP_001138779.1:n.-430G>A
NM_001145308.4:c.-612G>A (LRTOMT)	NP_001138780.1:n.-612G>A
NM_001145309.3:c.-833G>A (LRTOMT)	NP_001138781.1:n.-833G>A
NM_001145310.3:c.-833G>A (LRTOMT)	NP_001138782.1:n.-833G>A
NM_001205138.3:c.-347G>A (LRTOMT)	NP_001192067.1:n.-347G>A
NM_001271471.2:c.-430G>A (LRTOMT)	NP_001258400.1:n.-430G>A
NM_001286561.1:c.-338C>T (NUMA1)	NP_001273490.1:n.-338C>T
NM_006185.3:c.-240C>T (NUMA1)	NP_006176.2:n.-240C>T
NM_145309.5:c.-430G>A (LRTOMT)	NP_660352.1:n.-430G>A
NR_026886.3:n.265G>A (LRTOMT)
XM_011545055.1:c.-240C>T (NUMA1)	XP_011543357.1:n.-240C>T
NM_001318803.1:c.-387G>A (LRTOMT)	NP_001305732.1:n.-387G>A
NR_134858.1:n.265G>A (LRTOMT)
XM_006718474.4:c.-346G>A (LRTOMT)	XP_006718537.1:n.-346G>A