Canonical Allele Identifier: CA1981828424

Linked Data

dbSNP Id: rs1591116584

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080620A>G , CM000673.2:g.72080620A>G GRCh38
NC_000011.9:g.71791666A>G , CM000673.1:g.71791666A>G GRCh37
NC_000011.8:g.71469314A>G NCBI36
NG_021423.1:g.5285A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-405A>G (LRRC51) ENSP00000289488.2:n.-405A>G
ENST00000535883.6:c.-282A>G (LRRC51) ENSP00000437561.1:n.-282A>G
ENST00000538413.6:c.-321A>G (LRRC51) ENSP00000438762.2:n.-321A>G
ENST00000539271.6:c.-475A>G (LRRC51) ENSP00000442267.2:n.-475A>G
ENST00000642648.1:c.-282A>G (LRRC51) ENSP00000494362.1:n.-282A>G
ENST00000642813.1:n.55A>G (LRRC51)
ENST00000647530.1:c.-568A>G (LRRC51) ENSP00000494072.1:n.-568A>G
ENST00000307198.11:c.-587A>G (LRRC51) ENSP00000305742.7:n.-587A>G
ENST00000393695.7:c.-265T>C (NUMA1) ENSP00000377298.3:n.-265T>C
ENST00000535883.5:c.-405A>G (LRRC51) ENSP00000437561.1:n.-405A>G
ENST00000538413.5:c.-282A>G (LRRC51) ENSP00000438762.1:n.-282A>G
ENST00000543450.1:n.74T>C (NUMA1)
ENST00000613205.4:c.-265T>C (NUMA1) ENSP00000480172.1:n.-265T>C
NM_001145307.4:c.-405A>G (LRTOMT) NP_001138779.1:n.-405A>G
NM_001145308.4:c.-587A>G (LRTOMT) NP_001138780.1:n.-587A>G
NM_001145309.3:c.-808A>G (LRTOMT) NP_001138781.1:n.-808A>G
NM_001145310.3:c.-808A>G (LRTOMT) NP_001138782.1:n.-808A>G
NM_001205138.3:c.-322A>G (LRTOMT) NP_001192067.1:n.-322A>G
NM_001271471.2:c.-405A>G (LRTOMT) NP_001258400.1:n.-405A>G
NM_001286561.1:c.-363T>C (NUMA1) NP_001273490.1:n.-363T>C
NM_006185.3:c.-265T>C (NUMA1) NP_006176.2:n.-265T>C
NM_145309.5:c.-405A>G (LRTOMT) NP_660352.1:n.-405A>G
NR_026886.3:n.290A>G (LRTOMT)
XM_011545055.1:c.-265T>C (NUMA1) XP_011543357.1:n.-265T>C
NM_001318803.1:c.-362A>G (LRTOMT) NP_001305732.1:n.-362A>G
NR_134858.1:n.290A>G (LRTOMT)
XM_006718474.4:c.-321A>G (LRTOMT) XP_006718537.1:n.-321A>G
XM_011544848.3:c.-568A>G (LRTOMT) XP_011543150.1:n.-568A>G