Canonical Allele Identifier: CA2792647118

Gene: LRRC51 NUMA1 LRTOMT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080606del , CM000673.2:g.72080606del	GRCh38
NC_000011.9:g.71791652del , CM000673.1:g.71791652del	GRCh37
NC_000011.8:g.71469300del	NCBI36
NG_021423.1:g.5271del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-419del (LRRC51)	ENSP00000289488.2:n.-419del
ENST00000535883.6:c.-296del (LRRC51)	ENSP00000437561.1:n.-296del
ENST00000538413.6:c.-335del (LRRC51)	ENSP00000438762.2:n.-335del
ENST00000539271.6:c.-489del (LRRC51)	ENSP00000442267.2:n.-489del
ENST00000642648.1:c.-296del (LRRC51)	ENSP00000494362.1:n.-296del
ENST00000642813.1:n.41del (LRRC51)
ENST00000647530.1:c.-582del (LRRC51)	ENSP00000494072.1:n.-582del
ENST00000307198.11:c.-601del (LRRC51)	ENSP00000305742.7:n.-601del
ENST00000393695.7:c.-251del (NUMA1)	ENSP00000377298.3:n.-251del
ENST00000535883.5:c.-419del (LRRC51)	ENSP00000437561.1:n.-419del
ENST00000538413.5:c.-296del (LRRC51)	ENSP00000438762.1:n.-296del
ENST00000543450.1:n.88del (NUMA1)
ENST00000613205.4:c.-251del (NUMA1)	ENSP00000480172.1:n.-251del
NM_001145307.4:c.-419del (LRTOMT)	NP_001138779.1:n.-419del
NM_001145308.4:c.-601del (LRTOMT)	NP_001138780.1:n.-601del
NM_001145309.3:c.-822del (LRTOMT)	NP_001138781.1:n.-822del
NM_001145310.3:c.-822del (LRTOMT)	NP_001138782.1:n.-822del
NM_001205138.3:c.-336del (LRTOMT)	NP_001192067.1:n.-336del
NM_001271471.2:c.-419del (LRTOMT)	NP_001258400.1:n.-419del
NM_001286561.1:c.-349del (NUMA1)	NP_001273490.1:n.-349del
NM_006185.3:c.-251del (NUMA1)	NP_006176.2:n.-251del
NM_145309.5:c.-419del (LRTOMT)	NP_660352.1:n.-419del
NR_026886.3:n.276del (LRTOMT)
XM_011545055.1:c.-251del (NUMA1)	XP_011543357.1:n.-251del
NM_001318803.1:c.-376del (LRTOMT)	NP_001305732.1:n.-376del
NR_134858.1:n.276del (LRTOMT)
XM_006718474.4:c.-335del (LRTOMT)	XP_006718537.1:n.-335del
XM_011544848.3:c.-582del (LRTOMT)	XP_011543150.1:n.-582del