Canonical Allele Identifier: CA2229281074
Gene: LRRC36 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67375336C= , CM000678.2:g.67375336C= GRCh38
NC_000016.9:g.67409239C= , CM000678.1:g.67409239C= GRCh37
NC_000016.8:g.65966740C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000329956.11:c.1584C= MANE Select ENSP00000329943.6:p.Val528=
ENST00000329956.10:c.1584C= ENSP00000329943.6:p.Val528=
ENST00000435835.3:c.1132-3253C= ENSP00000411122.3:n.1132-3253C=
ENST00000563189.5:c.1221C= ENSP00000455103.1:p.Val407=
ENST00000565019.6:c.1093C=
ENST00000567723.5:c.*910C= ENSP00000455799.1:n.*910C=
ENST00000567823.5:c.*79C= ENSP00000456164.1:n.*79C=
ENST00000568010.5:c.*324C= ENSP00000455018.1:n.*324C=
NM_001161575.1:c.1221C= NP_001155047.1:p.Val407=
NM_018296.5:c.1584C= NP_060766.5:p.Val528=
XM_005256025.2:c.1584C= XP_005256082.1:p.Val528=
XM_005256026.2:c.1143C= XP_005256083.1:p.Val381=
XM_005256027.2:c.1584C= XP_005256084.1:p.Val528=
XM_005256028.1:c.1080C= XP_005256085.1:p.Val360=
XM_011523199.1:c.1584C= XP_011521501.1:p.Val528=
XM_011523200.1:c.1584C= XP_011521502.1:p.Val528=
XM_011523201.1:c.1080C= XP_011521503.1:p.Val360=
XM_011523202.1:c.1077C= XP_011521504.1:p.Val359=
XM_011523203.1:c.966C= XP_011521505.1:p.Val322=
XM_011523204.1:c.858C= XP_011521506.1:p.Val286=
XM_011523205.1:c.858C= XP_011521507.1:p.Val286=
XR_243416.2:n.1603C=
XR_429723.1:n.1592C=
XM_011523202.2:c.1077C= XP_011521504.1:p.Val359=
XM_017023400.2:c.1584C= XP_016878889.1:p.Val528=
XM_017023401.1:c.833C= XP_016878890.1:p.Ser278=
XM_017023402.1:c.656C= XP_016878891.1:p.Ser219=
XM_024450338.1:c.858C= XP_024306106.1:p.Val286=
NM_018296.6:c.1584C= MANE Select NP_060766.5:p.Val528=
NM_001161575.2:c.1221C= NP_001155047.1:p.Val407=