Canonical Allele Identifier: CA1981828468
Gene: LRRC51 HGNC NCBI
LRTOMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080697G= , CM000673.2:g.72080697G= GRCh38
NC_000011.9:g.71791743G= , CM000673.1:g.71791743G= GRCh37
NC_000011.8:g.71469391G= NCBI36
NG_021423.1:g.5362G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-328G= (LRRC51) ENSP00000289488.2:n.-328G=
ENST00000535883.6:c.-205G= (LRRC51) ENSP00000437561.1:n.-205G=
ENST00000538413.6:c.-244G= (LRRC51) ENSP00000438762.2:n.-244G=
ENST00000539271.6:c.-398G= (LRRC51) ENSP00000442267.2:n.-398G=
ENST00000642510.1:c.-521G= (LRRC51) ENSP00000496544.1:n.-521G=
ENST00000642648.1:c.-205G= (LRRC51) ENSP00000494362.1:n.-205G=
ENST00000642813.1:n.132G= (LRRC51)
ENST00000647530.1:c.-491G= (LRRC51) ENSP00000494072.1:n.-491G=
ENST00000289488.6:c.-328G= (LRRC51) ENSP00000289488.2:n.-328G=
ENST00000307198.11:c.-510G= (LRRC51) ENSP00000305742.7:n.-510G=
ENST00000535883.5:c.-328G= (LRRC51) ENSP00000437561.1:n.-328G=
ENST00000538413.5:c.-205G= (LRRC51) ENSP00000438762.1:n.-205G=
NM_001145307.4:c.-328G= (LRTOMT) NP_001138779.1:n.-328G=
NM_001145308.4:c.-510G= (LRTOMT) NP_001138780.1:n.-510G=
NM_001145309.3:c.-731G= (LRTOMT) NP_001138781.1:n.-731G=
NM_001145310.3:c.-731G= (LRTOMT) NP_001138782.1:n.-731G=
NM_001205138.3:c.-245G= (LRTOMT) NP_001192067.1:n.-245G=
NM_001271471.2:c.-328G= (LRTOMT) NP_001258400.1:n.-328G=
NM_145309.5:c.-328G= (LRTOMT) NP_660352.1:n.-328G=
NR_026886.3:n.367G= (LRTOMT)
XM_006718473.2:c.-205G= (LRTOMT) XP_006718536.1:n.-205G=
NM_001318803.1:c.-285G= (LRTOMT) NP_001305732.1:n.-285G=
NR_134858.1:n.367G= (LRTOMT)
XM_006718473.4:c.-205G= (LRTOMT) XP_006718536.1:n.-205G=
XM_006718474.4:c.-244G= (LRTOMT) XP_006718537.1:n.-244G=
XM_011544848.3:c.-491G= (LRTOMT) XP_011543150.1:n.-491G=