Canonical Allele Identifier: CA224380565

Linked Data

dbSNP Id: rs1039445978

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080658A>G , CM000673.2:g.72080658A>G GRCh38
NC_000011.9:g.71791704A>G , CM000673.1:g.71791704A>G GRCh37
NC_000011.8:g.71469352A>G NCBI36
NG_021423.1:g.5323A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-367A>G (LRRC51) ENSP00000289488.2:n.-367A>G
ENST00000535883.6:c.-244A>G (LRRC51) ENSP00000437561.1:n.-244A>G
ENST00000538413.6:c.-283A>G (LRRC51) ENSP00000438762.2:n.-283A>G
ENST00000539271.6:c.-437A>G (LRRC51) ENSP00000442267.2:n.-437A>G
ENST00000642648.1:c.-244A>G (LRRC51) ENSP00000494362.1:n.-244A>G
ENST00000642813.1:n.93A>G (LRRC51)
ENST00000647530.1:c.-530A>G (LRRC51) ENSP00000494072.1:n.-530A>G
ENST00000289488.6:c.-367A>G (LRRC51) ENSP00000289488.2:n.-367A>G
ENST00000307198.11:c.-549A>G (LRRC51) ENSP00000305742.7:n.-549A>G
ENST00000393695.7:c.-303T>C (NUMA1) ENSP00000377298.3:n.-303T>C
ENST00000535883.5:c.-367A>G (LRRC51) ENSP00000437561.1:n.-367A>G
ENST00000538413.5:c.-244A>G (LRRC51) ENSP00000438762.1:n.-244A>G
ENST00000543450.1:n.36T>C (NUMA1)
ENST00000613205.4:c.-303T>C (NUMA1) ENSP00000480172.1:n.-303T>C
NM_001145307.4:c.-367A>G (LRTOMT) NP_001138779.1:n.-367A>G
NM_001145308.4:c.-549A>G (LRTOMT) NP_001138780.1:n.-549A>G
NM_001145309.3:c.-770A>G (LRTOMT) NP_001138781.1:n.-770A>G
NM_001145310.3:c.-770A>G (LRTOMT) NP_001138782.1:n.-770A>G
NM_001205138.3:c.-284A>G (LRTOMT) NP_001192067.1:n.-284A>G
NM_001271471.2:c.-367A>G (LRTOMT) NP_001258400.1:n.-367A>G
NM_001286561.1:c.-401T>C (NUMA1) NP_001273490.1:n.-401T>C
NM_006185.3:c.-303T>C (NUMA1) NP_006176.2:n.-303T>C
NM_145309.5:c.-367A>G (LRTOMT) NP_660352.1:n.-367A>G
NR_026886.3:n.328A>G (LRTOMT)
XM_011545055.1:c.-303T>C (NUMA1) XP_011543357.1:n.-303T>C
NM_001318803.1:c.-324A>G (LRTOMT) NP_001305732.1:n.-324A>G
NR_134858.1:n.328A>G (LRTOMT)
XM_006718474.4:c.-283A>G (LRTOMT) XP_006718537.1:n.-283A>G
XM_011544848.3:c.-530A>G (LRTOMT) XP_011543150.1:n.-530A>G