Canonical Allele Identifier: CA2614916441

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080600G>T , CM000673.2:g.72080600G>T GRCh38
NC_000011.9:g.71791646G>T , CM000673.1:g.71791646G>T GRCh37
NC_000011.8:g.71469294G>T NCBI36
NG_021423.1:g.5265G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-425G>T (LRRC51) ENSP00000289488.2:n.-425G>T
ENST00000535883.6:c.-302G>T (LRRC51) ENSP00000437561.1:n.-302G>T
ENST00000538413.6:c.-341G>T (LRRC51) ENSP00000438762.2:n.-341G>T
ENST00000642648.1:c.-302G>T (LRRC51) ENSP00000494362.1:n.-302G>T
ENST00000642813.1:n.35G>T (LRRC51)
ENST00000647530.1:c.-588G>T (LRRC51) ENSP00000494072.1:n.-588G>T
ENST00000307198.11:c.-607G>T (LRRC51) ENSP00000305742.7:n.-607G>T
ENST00000393695.7:c.-245C>A (NUMA1) ENSP00000377298.3:n.-245C>A
ENST00000535883.5:c.-425G>T (LRRC51) ENSP00000437561.1:n.-425G>T
ENST00000538413.5:c.-302G>T (LRRC51) ENSP00000438762.1:n.-302G>T
ENST00000543450.1:n.94C>A (NUMA1)
ENST00000613205.4:c.-245C>A (NUMA1) ENSP00000480172.1:n.-245C>A
NM_001145307.4:c.-425G>T (LRTOMT) NP_001138779.1:n.-425G>T
NM_001145308.4:c.-607G>T (LRTOMT) NP_001138780.1:n.-607G>T
NM_001145309.3:c.-828G>T (LRTOMT) NP_001138781.1:n.-828G>T
NM_001145310.3:c.-828G>T (LRTOMT) NP_001138782.1:n.-828G>T
NM_001205138.3:c.-342G>T (LRTOMT) NP_001192067.1:n.-342G>T
NM_001271471.2:c.-425G>T (LRTOMT) NP_001258400.1:n.-425G>T
NM_001286561.1:c.-343C>A (NUMA1) NP_001273490.1:n.-343C>A
NM_006185.3:c.-245C>A (NUMA1) NP_006176.2:n.-245C>A
NM_145309.5:c.-425G>T (LRTOMT) NP_660352.1:n.-425G>T
NR_026886.3:n.270G>T (LRTOMT)
XM_011545055.1:c.-245C>A (NUMA1) XP_011543357.1:n.-245C>A
NM_001318803.1:c.-382G>T (LRTOMT) NP_001305732.1:n.-382G>T
NR_134858.1:n.270G>T (LRTOMT)
XM_006718474.4:c.-341G>T (LRTOMT) XP_006718537.1:n.-341G>T
XM_011544848.3:c.-588G>T (LRTOMT) XP_011543150.1:n.-588G>T