Canonical Allele Identifier: CA600079854

Gene: LRRC51 NUMA1 LRTOMT

Linked Data

• dbSNP Id: rs1286651011
• gnomAD v2: 11-71791694-G-A
• gnomAD v3: 11-72080648-G-A
• gnomAD v4: 11-72080648-G-A
• MyVariant Identifiers: chr11:g.71791694G>A (hg19) ; chr11:g.72080648G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080648G>A , CM000673.2:g.72080648G>A	GRCh38
NC_000011.9:g.71791694G>A , CM000673.1:g.71791694G>A	GRCh37
NC_000011.8:g.71469342G>A	NCBI36
NG_021423.1:g.5313G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-377G>A (LRRC51)	ENSP00000289488.2:n.-377G>A
ENST00000535883.6:c.-254G>A (LRRC51)	ENSP00000437561.1:n.-254G>A
ENST00000538413.6:c.-293G>A (LRRC51)	ENSP00000438762.2:n.-293G>A
ENST00000539271.6:c.-447G>A (LRRC51)	ENSP00000442267.2:n.-447G>A
ENST00000642648.1:c.-254G>A (LRRC51)	ENSP00000494362.1:n.-254G>A
ENST00000642813.1:n.83G>A (LRRC51)
ENST00000647530.1:c.-540G>A (LRRC51)	ENSP00000494072.1:n.-540G>A
ENST00000289488.6:c.-377G>A (LRRC51)	ENSP00000289488.2:n.-377G>A
ENST00000307198.11:c.-559G>A (LRRC51)	ENSP00000305742.7:n.-559G>A
ENST00000393695.7:c.-293C>T (NUMA1)	ENSP00000377298.3:n.-293C>T
ENST00000535883.5:c.-377G>A (LRRC51)	ENSP00000437561.1:n.-377G>A
ENST00000538413.5:c.-254G>A (LRRC51)	ENSP00000438762.1:n.-254G>A
ENST00000543450.1:n.46C>T (NUMA1)
ENST00000613205.4:c.-293C>T (NUMA1)	ENSP00000480172.1:n.-293C>T
NM_001145307.4:c.-377G>A (LRTOMT)	NP_001138779.1:n.-377G>A
NM_001145308.4:c.-559G>A (LRTOMT)	NP_001138780.1:n.-559G>A
NM_001145309.3:c.-780G>A (LRTOMT)	NP_001138781.1:n.-780G>A
NM_001145310.3:c.-780G>A (LRTOMT)	NP_001138782.1:n.-780G>A
NM_001205138.3:c.-294G>A (LRTOMT)	NP_001192067.1:n.-294G>A
NM_001271471.2:c.-377G>A (LRTOMT)	NP_001258400.1:n.-377G>A
NM_001286561.1:c.-391C>T (NUMA1)	NP_001273490.1:n.-391C>T
NM_006185.3:c.-293C>T (NUMA1)	NP_006176.2:n.-293C>T
NM_145309.5:c.-377G>A (LRTOMT)	NP_660352.1:n.-377G>A
NR_026886.3:n.318G>A (LRTOMT)
XM_011545055.1:c.-293C>T (NUMA1)	XP_011543357.1:n.-293C>T
NM_001318803.1:c.-334G>A (LRTOMT)	NP_001305732.1:n.-334G>A
NR_134858.1:n.318G>A (LRTOMT)
XM_006718474.4:c.-293G>A (LRTOMT)	XP_006718537.1:n.-293G>A
XM_011544848.3:c.-540G>A (LRTOMT)	XP_011543150.1:n.-540G>A