Canonical Allele Identifier: CA2614916510

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080689A>G , CM000673.2:g.72080689A>G GRCh38
NC_000011.9:g.71791735A>G , CM000673.1:g.71791735A>G GRCh37
NC_000011.8:g.71469383A>G NCBI36
NG_021423.1:g.5354A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-336A>G (LRRC51) ENSP00000289488.2:n.-336A>G
ENST00000535883.6:c.-213A>G (LRRC51) ENSP00000437561.1:n.-213A>G
ENST00000538413.6:c.-252A>G (LRRC51) ENSP00000438762.2:n.-252A>G
ENST00000539271.6:c.-406A>G (LRRC51) ENSP00000442267.2:n.-406A>G
ENST00000642510.1:c.-529A>G (LRRC51) ENSP00000496544.1:n.-529A>G
ENST00000642648.1:c.-213A>G (LRRC51) ENSP00000494362.1:n.-213A>G
ENST00000642813.1:n.124A>G (LRRC51)
ENST00000647530.1:c.-499A>G (LRRC51) ENSP00000494072.1:n.-499A>G
ENST00000289488.6:c.-336A>G (LRRC51) ENSP00000289488.2:n.-336A>G
ENST00000307198.11:c.-518A>G (LRRC51) ENSP00000305742.7:n.-518A>G
ENST00000535883.5:c.-336A>G (LRRC51) ENSP00000437561.1:n.-336A>G
ENST00000538413.5:c.-213A>G (LRRC51) ENSP00000438762.1:n.-213A>G
ENST00000543450.1:n.5T>C (NUMA1)
ENST00000613205.4:c.-334T>C (NUMA1) ENSP00000480172.1:n.-334T>C
NM_001145307.4:c.-336A>G (LRTOMT) NP_001138779.1:n.-336A>G
NM_001145308.4:c.-518A>G (LRTOMT) NP_001138780.1:n.-518A>G
NM_001145309.3:c.-739A>G (LRTOMT) NP_001138781.1:n.-739A>G
NM_001145310.3:c.-739A>G (LRTOMT) NP_001138782.1:n.-739A>G
NM_001205138.3:c.-253A>G (LRTOMT) NP_001192067.1:n.-253A>G
NM_001271471.2:c.-336A>G (LRTOMT) NP_001258400.1:n.-336A>G
NM_001286561.1:c.-432T>C (NUMA1) NP_001273490.1:n.-432T>C
NM_006185.3:c.-334T>C (NUMA1) NP_006176.2:n.-334T>C
NM_145309.5:c.-336A>G (LRTOMT) NP_660352.1:n.-336A>G
NR_026886.3:n.359A>G (LRTOMT)
XM_006718473.2:c.-213A>G (LRTOMT) XP_006718536.1:n.-213A>G
NM_001318803.1:c.-293A>G (LRTOMT) NP_001305732.1:n.-293A>G
NR_134858.1:n.359A>G (LRTOMT)
XM_006718473.4:c.-213A>G (LRTOMT) XP_006718536.1:n.-213A>G
XM_006718474.4:c.-252A>G (LRTOMT) XP_006718537.1:n.-252A>G
XM_011544848.3:c.-499A>G (LRTOMT) XP_011543150.1:n.-499A>G