Canonical Allele Identifier: CA2614916506

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080686T>C , CM000673.2:g.72080686T>C GRCh38
NC_000011.9:g.71791732T>C , CM000673.1:g.71791732T>C GRCh37
NC_000011.8:g.71469380T>C NCBI36
NG_021423.1:g.5351T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-339T>C (LRRC51) ENSP00000289488.2:n.-339T>C
ENST00000535883.6:c.-216T>C (LRRC51) ENSP00000437561.1:n.-216T>C
ENST00000538413.6:c.-255T>C (LRRC51) ENSP00000438762.2:n.-255T>C
ENST00000539271.6:c.-409T>C (LRRC51) ENSP00000442267.2:n.-409T>C
ENST00000642510.1:c.-532T>C (LRRC51) ENSP00000496544.1:n.-532T>C
ENST00000642648.1:c.-216T>C (LRRC51) ENSP00000494362.1:n.-216T>C
ENST00000642813.1:n.121T>C (LRRC51)
ENST00000647530.1:c.-502T>C (LRRC51) ENSP00000494072.1:n.-502T>C
ENST00000289488.6:c.-339T>C (LRRC51) ENSP00000289488.2:n.-339T>C
ENST00000307198.11:c.-521T>C (LRRC51) ENSP00000305742.7:n.-521T>C
ENST00000393695.7:c.-331A>G (NUMA1) ENSP00000377298.3:n.-331A>G
ENST00000535883.5:c.-339T>C (LRRC51) ENSP00000437561.1:n.-339T>C
ENST00000538413.5:c.-216T>C (LRRC51) ENSP00000438762.1:n.-216T>C
ENST00000543450.1:n.8A>G (NUMA1)
ENST00000613205.4:c.-331A>G (NUMA1) ENSP00000480172.1:n.-331A>G
NM_001145307.4:c.-339T>C (LRTOMT) NP_001138779.1:n.-339T>C
NM_001145308.4:c.-521T>C (LRTOMT) NP_001138780.1:n.-521T>C
NM_001145309.3:c.-742T>C (LRTOMT) NP_001138781.1:n.-742T>C
NM_001145310.3:c.-742T>C (LRTOMT) NP_001138782.1:n.-742T>C
NM_001205138.3:c.-256T>C (LRTOMT) NP_001192067.1:n.-256T>C
NM_001271471.2:c.-339T>C (LRTOMT) NP_001258400.1:n.-339T>C
NM_001286561.1:c.-429A>G (NUMA1) NP_001273490.1:n.-429A>G
NM_006185.3:c.-331A>G (NUMA1) NP_006176.2:n.-331A>G
NM_145309.5:c.-339T>C (LRTOMT) NP_660352.1:n.-339T>C
NR_026886.3:n.356T>C (LRTOMT)
XM_006718473.2:c.-216T>C (LRTOMT) XP_006718536.1:n.-216T>C
XM_011545055.1:c.-331A>G (NUMA1) XP_011543357.1:n.-331A>G
NM_001318803.1:c.-296T>C (LRTOMT) NP_001305732.1:n.-296T>C
NR_134858.1:n.356T>C (LRTOMT)
XM_006718473.4:c.-216T>C (LRTOMT) XP_006718536.1:n.-216T>C
XM_006718474.4:c.-255T>C (LRTOMT) XP_006718537.1:n.-255T>C
XM_011544848.3:c.-502T>C (LRTOMT) XP_011543150.1:n.-502T>C