Canonical Allele Identifier: CA1981828427

Gene: LRRC51 NUMA1 LRTOMT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080629T= , CM000673.2:g.72080629T=	GRCh38
NC_000011.9:g.71791675T= , CM000673.1:g.71791675T=	GRCh37
NC_000011.8:g.71469323T=	NCBI36
NG_021423.1:g.5294T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-396T= (LRRC51)	ENSP00000289488.2:n.-396T=
ENST00000535883.6:c.-273T= (LRRC51)	ENSP00000437561.1:n.-273T=
ENST00000538413.6:c.-312T= (LRRC51)	ENSP00000438762.2:n.-312T=
ENST00000539271.6:c.-466T= (LRRC51)	ENSP00000442267.2:n.-466T=
ENST00000642648.1:c.-273T= (LRRC51)	ENSP00000494362.1:n.-273T=
ENST00000642813.1:n.64T= (LRRC51)
ENST00000647530.1:c.-559T= (LRRC51)	ENSP00000494072.1:n.-559T=
ENST00000307198.11:c.-578T= (LRRC51)	ENSP00000305742.7:n.-578T=
ENST00000393695.7:c.-274A= (NUMA1)	ENSP00000377298.3:n.-274A=
ENST00000535883.5:c.-396T= (LRRC51)	ENSP00000437561.1:n.-396T=
ENST00000538413.5:c.-273T= (LRRC51)	ENSP00000438762.1:n.-273T=
ENST00000543450.1:n.65A= (NUMA1)
ENST00000613205.4:c.-274A= (NUMA1)	ENSP00000480172.1:n.-274A=
NM_001145307.4:c.-396T= (LRTOMT)	NP_001138779.1:n.-396T=
NM_001145308.4:c.-578T= (LRTOMT)	NP_001138780.1:n.-578T=
NM_001145309.3:c.-799T= (LRTOMT)	NP_001138781.1:n.-799T=
NM_001145310.3:c.-799T= (LRTOMT)	NP_001138782.1:n.-799T=
NM_001205138.3:c.-313T= (LRTOMT)	NP_001192067.1:n.-313T=
NM_001271471.2:c.-396T= (LRTOMT)	NP_001258400.1:n.-396T=
NM_001286561.1:c.-372A= (NUMA1)	NP_001273490.1:n.-372A=
NM_006185.3:c.-274A= (NUMA1)	NP_006176.2:n.-274A=
NM_145309.5:c.-396T= (LRTOMT)	NP_660352.1:n.-396T=
NR_026886.3:n.299T= (LRTOMT)
XM_011545055.1:c.-274A= (NUMA1)	XP_011543357.1:n.-274A=
NM_001318803.1:c.-353T= (LRTOMT)	NP_001305732.1:n.-353T=
NR_134858.1:n.299T= (LRTOMT)
XM_006718474.4:c.-312T= (LRTOMT)	XP_006718537.1:n.-312T=
XM_011544848.3:c.-559T= (LRTOMT)	XP_011543150.1:n.-559T=