Canonical Allele Identifier: CA1981828439

Gene: LRRC51 NUMA1 LRTOMT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080655G= , CM000673.2:g.72080655G=	GRCh38
NC_000011.9:g.71791701G= , CM000673.1:g.71791701G=	GRCh37
NC_000011.8:g.71469349G=	NCBI36
NG_021423.1:g.5320G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-370G= (LRRC51)	ENSP00000289488.2:n.-370G=
ENST00000535883.6:c.-247G= (LRRC51)	ENSP00000437561.1:n.-247G=
ENST00000538413.6:c.-286G= (LRRC51)	ENSP00000438762.2:n.-286G=
ENST00000539271.6:c.-440G= (LRRC51)	ENSP00000442267.2:n.-440G=
ENST00000642648.1:c.-247G= (LRRC51)	ENSP00000494362.1:n.-247G=
ENST00000642813.1:n.90G= (LRRC51)
ENST00000647530.1:c.-533G= (LRRC51)	ENSP00000494072.1:n.-533G=
ENST00000289488.6:c.-370G= (LRRC51)	ENSP00000289488.2:n.-370G=
ENST00000307198.11:c.-552G= (LRRC51)	ENSP00000305742.7:n.-552G=
ENST00000393695.7:c.-300C= (NUMA1)	ENSP00000377298.3:n.-300C=
ENST00000535883.5:c.-370G= (LRRC51)	ENSP00000437561.1:n.-370G=
ENST00000538413.5:c.-247G= (LRRC51)	ENSP00000438762.1:n.-247G=
ENST00000543450.1:n.39C= (NUMA1)
ENST00000613205.4:c.-300C= (NUMA1)	ENSP00000480172.1:n.-300C=
NM_001145307.4:c.-370G= (LRTOMT)	NP_001138779.1:n.-370G=
NM_001145308.4:c.-552G= (LRTOMT)	NP_001138780.1:n.-552G=
NM_001145309.3:c.-773G= (LRTOMT)	NP_001138781.1:n.-773G=
NM_001145310.3:c.-773G= (LRTOMT)	NP_001138782.1:n.-773G=
NM_001205138.3:c.-287G= (LRTOMT)	NP_001192067.1:n.-287G=
NM_001271471.2:c.-370G= (LRTOMT)	NP_001258400.1:n.-370G=
NM_001286561.1:c.-398C= (NUMA1)	NP_001273490.1:n.-398C=
NM_006185.3:c.-300C= (NUMA1)	NP_006176.2:n.-300C=
NM_145309.5:c.-370G= (LRTOMT)	NP_660352.1:n.-370G=
NR_026886.3:n.325G= (LRTOMT)
XM_011545055.1:c.-300C= (NUMA1)	XP_011543357.1:n.-300C=
NM_001318803.1:c.-327G= (LRTOMT)	NP_001305732.1:n.-327G=
NR_134858.1:n.325G= (LRTOMT)
XM_006718474.4:c.-286G= (LRTOMT)	XP_006718537.1:n.-286G=
XM_011544848.3:c.-533G= (LRTOMT)	XP_011543150.1:n.-533G=