Canonical Allele Identifier: CA918911691

Gene: LRRC51 LRTOMT

Linked Data

• dbSNP Id: rs1591117455

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080839_72080852del , CM000673.2:g.72080839_72080852del	GRCh38
NC_000011.9:g.71791885_71791898del , CM000673.1:g.71791885_71791898del	GRCh37
NC_000011.8:g.71469533_71469546del	NCBI36
NG_021423.1:g.5504_5517del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-186_-173del (LRRC51)	ENSP00000289488.2:n.-186_-173del
ENST00000535883.6:c.-140+77_-140+90del (LRRC51)	ENSP00000437561.1:n.-140+77_-140+90del
ENST00000536917.2:c.-143_-130del (LRRC51)	ENSP00000443421.1:n.-143_-130del
ENST00000538413.6:c.-102_-89del (LRRC51)	ENSP00000438762.2:n.-102_-89del
ENST00000539271.6:c.-333+77_-333+90del (LRRC51)	ENSP00000442267.2:n.-333+77_-333+90del
ENST00000539587.6:c.-173_-160del (LRRC51)	ENSP00000437649.2:n.-173_-160del
ENST00000642510.1:c.-379_-366del (LRRC51)	ENSP00000496544.1:n.-379_-366del
ENST00000642648.1:c.-140+77_-140+90del (LRRC51)	ENSP00000494362.1:n.-140+77_-140+90del
ENST00000642813.1:n.274_287del (LRRC51)
ENST00000646163.1:c.-379_-366del (LRTOMT)	ENSP00000494749.1:n.-379_-366del
ENST00000647530.1:c.-349_-336del (LRRC51)	ENSP00000494072.1:n.-349_-336del
ENST00000289488.6:c.-186_-173del (LRRC51)	ENSP00000289488.2:n.-186_-173del
ENST00000307198.11:c.-368_-355del (LRRC51)	ENSP00000305742.7:n.-368_-355del
ENST00000412777.6:n.63_76del (LRRC51)
ENST00000423494.6:c.-103_-90del (LRRC51)	ENSP00000441249.1:n.-103_-90del
ENST00000535883.5:c.-186_-173del (LRRC51)	ENSP00000437561.1:n.-186_-173del
ENST00000538413.5:c.-140+77_-140+90del (LRRC51)	ENSP00000438762.1:n.-140+77_-140+90del
ENST00000539271.5:c.-368_-355del (LRRC51)	ENSP00000442267.1:n.-368_-355del
ENST00000539587.5:c.-162_-149del (LRRC51)	ENSP00000437649.1:n.-162_-149del
NM_001145307.4:c.-186_-173del (LRTOMT)	NP_001138779.1:n.-186_-173del
NM_001145308.4:c.-368_-355del (LRTOMT)	NP_001138780.1:n.-368_-355del
NM_001145309.3:c.-589_-576del (LRTOMT)	NP_001138781.1:n.-589_-576del
NM_001145310.3:c.-589_-576del (LRTOMT)	NP_001138782.1:n.-589_-576del
NM_001205138.3:c.-103_-90del (LRTOMT)	NP_001192067.1:n.-103_-90del
NM_001271471.2:c.-186_-173del (LRTOMT)	NP_001258400.1:n.-186_-173del
NM_145309.5:c.-186_-173del (LRTOMT)	NP_660352.1:n.-186_-173del
NR_026886.3:n.509_522del (LRTOMT)
XM_006718472.2:c.-143_-130del (LRTOMT)	XP_006718535.1:n.-143_-130del
XM_006718473.2:c.-140+77_-140+90del (LRTOMT)	XP_006718536.1:n.-140+77_-140+90del
XM_006718474.2:c.-102_-89del (LRTOMT)	XP_006718537.1:n.-102_-89del
XM_011544847.1:c.-291_-278del (LRTOMT)	XP_011543149.1:n.-291_-278del
XM_011544848.1:c.-349_-336del (LRTOMT)	XP_011543150.1:n.-349_-336del
NM_001318803.1:c.-143_-130del (LRTOMT)	NP_001305732.1:n.-143_-130del
NR_134858.1:n.509_522del (LRTOMT)
XM_006718473.4:c.-140+77_-140+90del (LRTOMT)	XP_006718536.1:n.-140+77_-140+90del
XM_006718474.4:c.-102_-89del (LRTOMT)	XP_006718537.1:n.-102_-89del
XM_011544847.3:c.-291_-278del (LRTOMT)	XP_011543149.1:n.-291_-278del
XM_011544848.3:c.-349_-336del (LRTOMT)	XP_011543150.1:n.-349_-336del