Canonical Allele Identifier: CA1981828436

Gene: LRRC51 NUMA1 LRTOMT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080650G= , CM000673.2:g.72080650G=	GRCh38
NC_000011.9:g.71791696G= , CM000673.1:g.71791696G=	GRCh37
NC_000011.8:g.71469344G=	NCBI36
NG_021423.1:g.5315G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-375G= (LRRC51)	ENSP00000289488.2:n.-375G=
ENST00000535883.6:c.-252G= (LRRC51)	ENSP00000437561.1:n.-252G=
ENST00000538413.6:c.-291G= (LRRC51)	ENSP00000438762.2:n.-291G=
ENST00000539271.6:c.-445G= (LRRC51)	ENSP00000442267.2:n.-445G=
ENST00000642648.1:c.-252G= (LRRC51)	ENSP00000494362.1:n.-252G=
ENST00000642813.1:n.85G= (LRRC51)
ENST00000647530.1:c.-538G= (LRRC51)	ENSP00000494072.1:n.-538G=
ENST00000289488.6:c.-375G= (LRRC51)	ENSP00000289488.2:n.-375G=
ENST00000307198.11:c.-557G= (LRRC51)	ENSP00000305742.7:n.-557G=
ENST00000393695.7:c.-295C= (NUMA1)	ENSP00000377298.3:n.-295C=
ENST00000535883.5:c.-375G= (LRRC51)	ENSP00000437561.1:n.-375G=
ENST00000538413.5:c.-252G= (LRRC51)	ENSP00000438762.1:n.-252G=
ENST00000543450.1:n.44C= (NUMA1)
ENST00000613205.4:c.-295C= (NUMA1)	ENSP00000480172.1:n.-295C=
NM_001145307.4:c.-375G= (LRTOMT)	NP_001138779.1:n.-375G=
NM_001145308.4:c.-557G= (LRTOMT)	NP_001138780.1:n.-557G=
NM_001145309.3:c.-778G= (LRTOMT)	NP_001138781.1:n.-778G=
NM_001145310.3:c.-778G= (LRTOMT)	NP_001138782.1:n.-778G=
NM_001205138.3:c.-292G= (LRTOMT)	NP_001192067.1:n.-292G=
NM_001271471.2:c.-375G= (LRTOMT)	NP_001258400.1:n.-375G=
NM_001286561.1:c.-393C= (NUMA1)	NP_001273490.1:n.-393C=
NM_006185.3:c.-295C= (NUMA1)	NP_006176.2:n.-295C=
NM_145309.5:c.-375G= (LRTOMT)	NP_660352.1:n.-375G=
NR_026886.3:n.320G= (LRTOMT)
XM_011545055.1:c.-295C= (NUMA1)	XP_011543357.1:n.-295C=
NM_001318803.1:c.-332G= (LRTOMT)	NP_001305732.1:n.-332G=
NR_134858.1:n.320G= (LRTOMT)
XM_006718474.4:c.-291G= (LRTOMT)	XP_006718537.1:n.-291G=
XM_011544848.3:c.-538G= (LRTOMT)	XP_011543150.1:n.-538G=