Canonical Allele Identifier: CA396270055
Gene: LRRC36 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67375371G>T , CM000678.2:g.67375371G>T GRCh38
NC_000016.9:g.67409274G>T , CM000678.1:g.67409274G>T GRCh37
NC_000016.8:g.65966775G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000329956.11:c.1619G>T MANE Select ENSP00000329943.6:p.Trp540Leu
ENST00000329956.10:c.1619G>T ENSP00000329943.6:p.Trp540Leu
ENST00000435835.3:c.1132-3218G>T ENSP00000411122.3:n.1132-3218G>T
ENST00000563189.5:c.1256G>T ENSP00000455103.1:p.Trp419Leu
ENST00000565019.6:c.1128G>T
ENST00000567723.5:c.*945G>T ENSP00000455799.1:n.*945G>T
ENST00000567823.5:c.*114G>T ENSP00000456164.1:n.*114G>T
ENST00000568010.5:c.*359G>T ENSP00000455018.1:n.*359G>T
NM_001161575.1:c.1256G>T NP_001155047.1:p.Trp419Leu
NM_018296.5:c.1619G>T NP_060766.5:p.Trp540Leu
XM_005256025.2:c.1619G>T XP_005256082.1:p.Trp540Leu
XM_005256026.2:c.1178G>T XP_005256083.1:p.Trp393Leu
XM_005256027.2:c.1619G>T XP_005256084.1:p.Trp540Leu
XM_005256028.1:c.1115G>T XP_005256085.1:p.Trp372Leu
XM_011523199.1:c.1619G>T XP_011521501.1:p.Trp540Leu
XM_011523200.1:c.1619G>T XP_011521502.1:p.Trp540Leu
XM_011523201.1:c.1115G>T XP_011521503.1:p.Trp372Leu
XM_011523202.1:c.1112G>T XP_011521504.1:p.Trp371Leu
XM_011523203.1:c.1001G>T XP_011521505.1:p.Trp334Leu
XM_011523204.1:c.893G>T XP_011521506.1:p.Trp298Leu
XM_011523205.1:c.893G>T XP_011521507.1:p.Trp298Leu
XR_243416.2:n.1638G>T
XR_429723.1:n.1627G>T
XM_011523202.2:c.1112G>T XP_011521504.1:p.Trp371Leu
XM_017023400.2:c.1619G>T XP_016878889.1:p.Trp540Leu
XM_017023401.1:c.868G>T XP_016878890.1:p.Gly290Ter
XM_017023402.1:c.691G>T XP_016878891.1:p.Gly231Ter
XM_024450338.1:c.893G>T XP_024306106.1:p.Trp298Leu
NM_018296.6:c.1619G>T MANE Select NP_060766.5:p.Trp540Leu
NM_001161575.2:c.1256G>T NP_001155047.1:p.Trp419Leu