Canonical Allele Identifier: CA723037212
Gene: LRRC36 HGNC NCBI

Linked Data

dbSNP Id: rs760522273

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67375226dup , CM000678.2:g.67375226dup GRCh38
NC_000016.9:g.67409129dup , CM000678.1:g.67409129dup GRCh37
NC_000016.8:g.65966630dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000329956.11:c.1495-21dup MANE Select ENSP00000329943.6:n.1495-21dup
ENST00000329956.10:c.1495-21dup ENSP00000329943.6:n.1495-21dup
ENST00000435835.3:c.1132-3363dup ENSP00000411122.3:n.1132-3363dup
ENST00000563189.5:c.1132-21dup ENSP00000455103.1:n.1132-21dup
ENST00000565019.6:c.1072-89dup
ENST00000567723.5:c.*821-21dup ENSP00000455799.1:n.*821-21dup
ENST00000567823.5:c.215-21dup ENSP00000456164.1:n.215-21dup
ENST00000568010.5:c.*246-32dup ENSP00000455018.1:n.*246-32dup
NM_001161575.1:c.1132-21dup NP_001155047.1:n.1132-21dup
NM_018296.5:c.1495-21dup NP_060766.5:n.1495-21dup
XM_005256025.2:c.1495-21dup XP_005256082.1:n.1495-21dup
XM_005256026.2:c.1054-21dup XP_005256083.1:n.1054-21dup
XM_005256027.2:c.1495-21dup XP_005256084.1:n.1495-21dup
XM_005256028.1:c.991-21dup XP_005256085.1:n.991-21dup
XM_011523199.1:c.1495-21dup XP_011521501.1:n.1495-21dup
XM_011523200.1:c.1495-21dup XP_011521502.1:n.1495-21dup
XM_011523201.1:c.991-21dup XP_011521503.1:n.991-21dup
XM_011523202.1:c.988-21dup XP_011521504.1:n.988-21dup
XM_011523203.1:c.877-21dup XP_011521505.1:n.877-21dup
XM_011523204.1:c.769-21dup XP_011521506.1:n.769-21dup
XM_011523205.1:c.769-21dup XP_011521507.1:n.769-21dup
XR_243416.2:n.1514-21dup
XR_429723.1:n.1514-32dup
XM_011523202.2:c.988-21dup XP_011521504.1:n.988-21dup
XM_017023400.2:c.1495-21dup XP_016878889.1:n.1495-21dup
XM_017023401.1:c.755-32dup XP_016878890.1:n.755-32dup
XM_017023402.1:c.578-32dup XP_016878891.1:n.578-32dup
XM_024450338.1:c.769-21dup XP_024306106.1:n.769-21dup
NM_018296.6:c.1495-21dup MANE Select NP_060766.5:n.1495-21dup
NM_001161575.2:c.1132-21dup NP_001155047.1:n.1132-21dup