Canonical Allele Identifier: CA2614916539
Gene: LRRC51 HGNC NCBI
LRTOMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080713A>G , CM000673.2:g.72080713A>G GRCh38
NC_000011.9:g.71791759A>G , CM000673.1:g.71791759A>G GRCh37
NC_000011.8:g.71469407A>G NCBI36
NG_021423.1:g.5378A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-312A>G (LRRC51) ENSP00000289488.2:n.-312A>G
ENST00000535883.6:c.-189A>G (LRRC51) ENSP00000437561.1:n.-189A>G
ENST00000538413.6:c.-228A>G (LRRC51) ENSP00000438762.2:n.-228A>G
ENST00000539271.6:c.-382A>G (LRRC51) ENSP00000442267.2:n.-382A>G
ENST00000642510.1:c.-505A>G (LRRC51) ENSP00000496544.1:n.-505A>G
ENST00000642648.1:c.-189A>G (LRRC51) ENSP00000494362.1:n.-189A>G
ENST00000642813.1:n.148A>G (LRRC51)
ENST00000647530.1:c.-475A>G (LRRC51) ENSP00000494072.1:n.-475A>G
ENST00000289488.6:c.-312A>G (LRRC51) ENSP00000289488.2:n.-312A>G
ENST00000307198.11:c.-494A>G (LRRC51) ENSP00000305742.7:n.-494A>G
ENST00000535883.5:c.-312A>G (LRRC51) ENSP00000437561.1:n.-312A>G
ENST00000538413.5:c.-189A>G (LRRC51) ENSP00000438762.1:n.-189A>G
NM_001145307.4:c.-312A>G (LRTOMT) NP_001138779.1:n.-312A>G
NM_001145308.4:c.-494A>G (LRTOMT) NP_001138780.1:n.-494A>G
NM_001145309.3:c.-715A>G (LRTOMT) NP_001138781.1:n.-715A>G
NM_001145310.3:c.-715A>G (LRTOMT) NP_001138782.1:n.-715A>G
NM_001205138.3:c.-229A>G (LRTOMT) NP_001192067.1:n.-229A>G
NM_001271471.2:c.-312A>G (LRTOMT) NP_001258400.1:n.-312A>G
NM_145309.5:c.-312A>G (LRTOMT) NP_660352.1:n.-312A>G
NR_026886.3:n.383A>G (LRTOMT)
XM_006718473.2:c.-189A>G (LRTOMT) XP_006718536.1:n.-189A>G
NM_001318803.1:c.-269A>G (LRTOMT) NP_001305732.1:n.-269A>G
NR_134858.1:n.383A>G (LRTOMT)
XM_006718473.4:c.-189A>G (LRTOMT) XP_006718536.1:n.-189A>G
XM_006718474.4:c.-228A>G (LRTOMT) XP_006718537.1:n.-228A>G
XM_011544848.3:c.-475A>G (LRTOMT) XP_011543150.1:n.-475A>G