Canonical Allele Identifier: CA1981828459

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080683T= , CM000673.2:g.72080683T= GRCh38
NC_000011.9:g.71791729T= , CM000673.1:g.71791729T= GRCh37
NC_000011.8:g.71469377T= NCBI36
NG_021423.1:g.5348T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-342T= (LRRC51) ENSP00000289488.2:n.-342T=
ENST00000535883.6:c.-219T= (LRRC51) ENSP00000437561.1:n.-219T=
ENST00000538413.6:c.-258T= (LRRC51) ENSP00000438762.2:n.-258T=
ENST00000539271.6:c.-412T= (LRRC51) ENSP00000442267.2:n.-412T=
ENST00000642510.1:c.-535T= (LRRC51) ENSP00000496544.1:n.-535T=
ENST00000642648.1:c.-219T= (LRRC51) ENSP00000494362.1:n.-219T=
ENST00000642813.1:n.118T= (LRRC51)
ENST00000647530.1:c.-505T= (LRRC51) ENSP00000494072.1:n.-505T=
ENST00000289488.6:c.-342T= (LRRC51) ENSP00000289488.2:n.-342T=
ENST00000307198.11:c.-524T= (LRRC51) ENSP00000305742.7:n.-524T=
ENST00000393695.7:c.-328A= (NUMA1) ENSP00000377298.3:n.-328A=
ENST00000535883.5:c.-342T= (LRRC51) ENSP00000437561.1:n.-342T=
ENST00000538413.5:c.-219T= (LRRC51) ENSP00000438762.1:n.-219T=
ENST00000543450.1:n.11A= (NUMA1)
ENST00000613205.4:c.-328A= (NUMA1) ENSP00000480172.1:n.-328A=
NM_001145307.4:c.-342T= (LRTOMT) NP_001138779.1:n.-342T=
NM_001145308.4:c.-524T= (LRTOMT) NP_001138780.1:n.-524T=
NM_001145309.3:c.-745T= (LRTOMT) NP_001138781.1:n.-745T=
NM_001145310.3:c.-745T= (LRTOMT) NP_001138782.1:n.-745T=
NM_001205138.3:c.-259T= (LRTOMT) NP_001192067.1:n.-259T=
NM_001271471.2:c.-342T= (LRTOMT) NP_001258400.1:n.-342T=
NM_001286561.1:c.-426A= (NUMA1) NP_001273490.1:n.-426A=
NM_006185.3:c.-328A= (NUMA1) NP_006176.2:n.-328A=
NM_145309.5:c.-342T= (LRTOMT) NP_660352.1:n.-342T=
NR_026886.3:n.353T= (LRTOMT)
XM_006718473.2:c.-219T= (LRTOMT) XP_006718536.1:n.-219T=
XM_011545055.1:c.-328A= (NUMA1) XP_011543357.1:n.-328A=
NM_001318803.1:c.-299T= (LRTOMT) NP_001305732.1:n.-299T=
NR_134858.1:n.353T= (LRTOMT)
XM_006718473.4:c.-219T= (LRTOMT) XP_006718536.1:n.-219T=
XM_006718474.4:c.-258T= (LRTOMT) XP_006718537.1:n.-258T=
XM_011544848.3:c.-505T= (LRTOMT) XP_011543150.1:n.-505T=