Canonical Allele Identifier: CA1981828493
Gene: LRRC51 HGNC NCBI
LRTOMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080752T= , CM000673.2:g.72080752T= GRCh38
NC_000011.9:g.71791798T= , CM000673.1:g.71791798T= GRCh37
NC_000011.8:g.71469446T= NCBI36
NG_021423.1:g.5417T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-273T= (LRRC51) ENSP00000289488.2:n.-273T=
ENST00000535883.6:c.-150T= (LRRC51) ENSP00000437561.1:n.-150T=
ENST00000538413.6:c.-189T= (LRRC51) ENSP00000438762.2:n.-189T=
ENST00000539271.6:c.-343T= (LRRC51) ENSP00000442267.2:n.-343T=
ENST00000642510.1:c.-466T= (LRRC51) ENSP00000496544.1:n.-466T=
ENST00000642648.1:c.-150T= (LRRC51) ENSP00000494362.1:n.-150T=
ENST00000642813.1:n.187T= (LRRC51)
ENST00000647530.1:c.-436T= (LRRC51) ENSP00000494072.1:n.-436T=
ENST00000289488.6:c.-273T= (LRRC51) ENSP00000289488.2:n.-273T=
ENST00000307198.11:c.-455T= (LRRC51) ENSP00000305742.7:n.-455T=
ENST00000535883.5:c.-273T= (LRRC51) ENSP00000437561.1:n.-273T=
ENST00000538413.5:c.-150T= (LRRC51) ENSP00000438762.1:n.-150T=
NM_001145307.4:c.-273T= (LRTOMT) NP_001138779.1:n.-273T=
NM_001145308.4:c.-455T= (LRTOMT) NP_001138780.1:n.-455T=
NM_001145309.3:c.-676T= (LRTOMT) NP_001138781.1:n.-676T=
NM_001145310.3:c.-676T= (LRTOMT) NP_001138782.1:n.-676T=
NM_001205138.3:c.-190T= (LRTOMT) NP_001192067.1:n.-190T=
NM_001271471.2:c.-273T= (LRTOMT) NP_001258400.1:n.-273T=
NM_145309.5:c.-273T= (LRTOMT) NP_660352.1:n.-273T=
NR_026886.3:n.422T= (LRTOMT)
XM_006718473.2:c.-150T= (LRTOMT) XP_006718536.1:n.-150T=
NM_001318803.1:c.-230T= (LRTOMT) NP_001305732.1:n.-230T=
NR_134858.1:n.422T= (LRTOMT)
XM_006718473.4:c.-150T= (LRTOMT) XP_006718536.1:n.-150T=
XM_006718474.4:c.-189T= (LRTOMT) XP_006718537.1:n.-189T=
XM_011544848.3:c.-436T= (LRTOMT) XP_011543150.1:n.-436T=