Canonical Allele Identifier: CA2614916446

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080604C>T , CM000673.2:g.72080604C>T GRCh38
NC_000011.9:g.71791650C>T , CM000673.1:g.71791650C>T GRCh37
NC_000011.8:g.71469298C>T NCBI36
NG_021423.1:g.5269C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-421C>T (LRRC51) ENSP00000289488.2:n.-421C>T
ENST00000535883.6:c.-298C>T (LRRC51) ENSP00000437561.1:n.-298C>T
ENST00000538413.6:c.-337C>T (LRRC51) ENSP00000438762.2:n.-337C>T
ENST00000642648.1:c.-298C>T (LRRC51) ENSP00000494362.1:n.-298C>T
ENST00000642813.1:n.39C>T (LRRC51)
ENST00000647530.1:c.-584C>T (LRRC51) ENSP00000494072.1:n.-584C>T
ENST00000307198.11:c.-603C>T (LRRC51) ENSP00000305742.7:n.-603C>T
ENST00000393695.7:c.-249G>A (NUMA1) ENSP00000377298.3:n.-249G>A
ENST00000535883.5:c.-421C>T (LRRC51) ENSP00000437561.1:n.-421C>T
ENST00000538413.5:c.-298C>T (LRRC51) ENSP00000438762.1:n.-298C>T
ENST00000543450.1:n.90G>A (NUMA1)
ENST00000613205.4:c.-249G>A (NUMA1) ENSP00000480172.1:n.-249G>A
NM_001145307.4:c.-421C>T (LRTOMT) NP_001138779.1:n.-421C>T
NM_001145308.4:c.-603C>T (LRTOMT) NP_001138780.1:n.-603C>T
NM_001145309.3:c.-824C>T (LRTOMT) NP_001138781.1:n.-824C>T
NM_001145310.3:c.-824C>T (LRTOMT) NP_001138782.1:n.-824C>T
NM_001205138.3:c.-338C>T (LRTOMT) NP_001192067.1:n.-338C>T
NM_001271471.2:c.-421C>T (LRTOMT) NP_001258400.1:n.-421C>T
NM_001286561.1:c.-347G>A (NUMA1) NP_001273490.1:n.-347G>A
NM_006185.3:c.-249G>A (NUMA1) NP_006176.2:n.-249G>A
NM_145309.5:c.-421C>T (LRTOMT) NP_660352.1:n.-421C>T
NR_026886.3:n.274C>T (LRTOMT)
XM_011545055.1:c.-249G>A (NUMA1) XP_011543357.1:n.-249G>A
NM_001318803.1:c.-378C>T (LRTOMT) NP_001305732.1:n.-378C>T
NR_134858.1:n.274C>T (LRTOMT)
XM_006718474.4:c.-337C>T (LRTOMT) XP_006718537.1:n.-337C>T
XM_011544848.3:c.-584C>T (LRTOMT) XP_011543150.1:n.-584C>T