Canonical Allele Identifier: CA1981828435

Gene: LRRC51 NUMA1 LRTOMT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080650_72080657delinsGAAGGGGT , CM000673.2:g.72080650_72080657delinsGAAGGGGT	GRCh38
NC_000011.9:g.71791696_71791703delinsGAAGGGGT , CM000673.1:g.71791696_71791703delinsGAAGGGGT	GRCh37
NC_000011.8:g.71469344_71469351delinsGAAGGGGT	NCBI36
NG_021423.1:g.5315_5322delinsGAAGGGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-375_-368delinsGAAGGGGT (LRRC51)	ENSP00000289488.2:n.-375_-368delinsGAAGGGGT
ENST00000535883.6:c.-252_-245delinsGAAGGGGT (LRRC51)	ENSP00000437561.1:n.-252_-245delinsGAAGGGGT
ENST00000538413.6:c.-291_-284delinsGAAGGGGT (LRRC51)	ENSP00000438762.2:n.-291_-284delinsGAAGGGGT
ENST00000539271.6:c.-445_-438delinsGAAGGGGT (LRRC51)	ENSP00000442267.2:n.-445_-438delinsGAAGGGGT
ENST00000642648.1:c.-252_-245delinsGAAGGGGT (LRRC51)	ENSP00000494362.1:n.-252_-245delinsGAAGGGGT
ENST00000642813.1:n.85_92delinsGAAGGGGT (LRRC51)
ENST00000647530.1:c.-538_-531delinsGAAGGGGT (LRRC51)	ENSP00000494072.1:n.-538_-531delinsGAAGGGGT
ENST00000289488.6:c.-375_-368delinsGAAGGGGT (LRRC51)	ENSP00000289488.2:n.-375_-368delinsGAAGGGGT
ENST00000307198.11:c.-557_-550delinsGAAGGGGT (LRRC51)	ENSP00000305742.7:n.-557_-550delinsGAAGGGGT
ENST00000393695.7:c.-302_-295delinsACCCCTTC (NUMA1)	ENSP00000377298.3:n.-302_-295delinsACCCCTTC
ENST00000535883.5:c.-375_-368delinsGAAGGGGT (LRRC51)	ENSP00000437561.1:n.-375_-368delinsGAAGGGGT
ENST00000538413.5:c.-252_-245delinsGAAGGGGT (LRRC51)	ENSP00000438762.1:n.-252_-245delinsGAAGGGGT
ENST00000543450.1:n.37_44delinsACCCCTTC (NUMA1)
ENST00000613205.4:c.-302_-295delinsACCCCTTC (NUMA1)	ENSP00000480172.1:n.-302_-295delinsACCCCTTC
NM_001145307.4:c.-375_-368delinsGAAGGGGT (LRTOMT)	NP_001138779.1:n.-375_-368delinsGAAGGGGT
NM_001145308.4:c.-557_-550delinsGAAGGGGT (LRTOMT)	NP_001138780.1:n.-557_-550delinsGAAGGGGT
NM_001145309.3:c.-778_-771delinsGAAGGGGT (LRTOMT)	NP_001138781.1:n.-778_-771delinsGAAGGGGT
NM_001145310.3:c.-778_-771delinsGAAGGGGT (LRTOMT)	NP_001138782.1:n.-778_-771delinsGAAGGGGT
NM_001205138.3:c.-292_-285delinsGAAGGGGT (LRTOMT)	NP_001192067.1:n.-292_-285delinsGAAGGGGT
NM_001271471.2:c.-375_-368delinsGAAGGGGT (LRTOMT)	NP_001258400.1:n.-375_-368delinsGAAGGGGT
NM_001286561.1:c.-400_-393delinsACCCCTTC (NUMA1)	NP_001273490.1:n.-400_-393delinsACCCCTTC
NM_006185.3:c.-302_-295delinsACCCCTTC (NUMA1)	NP_006176.2:n.-302_-295delinsACCCCTTC
NM_145309.5:c.-375_-368delinsGAAGGGGT (LRTOMT)	NP_660352.1:n.-375_-368delinsGAAGGGGT
NR_026886.3:n.320_327delinsGAAGGGGT (LRTOMT)
XM_011545055.1:c.-302_-295delinsACCCCTTC (NUMA1)	XP_011543357.1:n.-302_-295delinsACCCCTTC
NM_001318803.1:c.-332_-325delinsGAAGGGGT (LRTOMT)	NP_001305732.1:n.-332_-325delinsGAAGGGGT
NR_134858.1:n.320_327delinsGAAGGGGT (LRTOMT)
XM_006718474.4:c.-291_-284delinsGAAGGGGT (LRTOMT)	XP_006718537.1:n.-291_-284delinsGAAGGGGT
XM_011544848.3:c.-538_-531delinsGAAGGGGT (LRTOMT)	XP_011543150.1:n.-538_-531delinsGAAGGGGT