Canonical Allele Identifier: CA2614916514

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72080691G>T , CM000673.2:g.72080691G>T GRCh38
NC_000011.9:g.71791737G>T , CM000673.1:g.71791737G>T GRCh37
NC_000011.8:g.71469385G>T NCBI36
NG_021423.1:g.5356G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000289488.7:c.-334G>T (LRRC51) ENSP00000289488.2:n.-334G>T
ENST00000535883.6:c.-211G>T (LRRC51) ENSP00000437561.1:n.-211G>T
ENST00000538413.6:c.-250G>T (LRRC51) ENSP00000438762.2:n.-250G>T
ENST00000539271.6:c.-404G>T (LRRC51) ENSP00000442267.2:n.-404G>T
ENST00000642510.1:c.-527G>T (LRRC51) ENSP00000496544.1:n.-527G>T
ENST00000642648.1:c.-211G>T (LRRC51) ENSP00000494362.1:n.-211G>T
ENST00000642813.1:n.126G>T (LRRC51)
ENST00000647530.1:c.-497G>T (LRRC51) ENSP00000494072.1:n.-497G>T
ENST00000289488.6:c.-334G>T (LRRC51) ENSP00000289488.2:n.-334G>T
ENST00000307198.11:c.-516G>T (LRRC51) ENSP00000305742.7:n.-516G>T
ENST00000535883.5:c.-334G>T (LRRC51) ENSP00000437561.1:n.-334G>T
ENST00000538413.5:c.-211G>T (LRRC51) ENSP00000438762.1:n.-211G>T
ENST00000543450.1:n.3C>A (NUMA1)
ENST00000613205.4:c.-336C>A (NUMA1) ENSP00000480172.1:n.-336C>A
NM_001145307.4:c.-334G>T (LRTOMT) NP_001138779.1:n.-334G>T
NM_001145308.4:c.-516G>T (LRTOMT) NP_001138780.1:n.-516G>T
NM_001145309.3:c.-737G>T (LRTOMT) NP_001138781.1:n.-737G>T
NM_001145310.3:c.-737G>T (LRTOMT) NP_001138782.1:n.-737G>T
NM_001205138.3:c.-251G>T (LRTOMT) NP_001192067.1:n.-251G>T
NM_001271471.2:c.-334G>T (LRTOMT) NP_001258400.1:n.-334G>T
NM_001286561.1:c.-434C>A (NUMA1) NP_001273490.1:n.-434C>A
NM_006185.3:c.-336C>A (NUMA1) NP_006176.2:n.-336C>A
NM_145309.5:c.-334G>T (LRTOMT) NP_660352.1:n.-334G>T
NR_026886.3:n.361G>T (LRTOMT)
XM_006718473.2:c.-211G>T (LRTOMT) XP_006718536.1:n.-211G>T
NM_001318803.1:c.-291G>T (LRTOMT) NP_001305732.1:n.-291G>T
NR_134858.1:n.361G>T (LRTOMT)
XM_006718473.4:c.-211G>T (LRTOMT) XP_006718536.1:n.-211G>T
XM_006718474.4:c.-250G>T (LRTOMT) XP_006718537.1:n.-250G>T
XM_011544848.3:c.-497G>T (LRTOMT) XP_011543150.1:n.-497G>T