Canonical Allele Identifier: CA919730191
Gene: LRRC36 HGNC NCBI

Linked Data

dbSNP Id: rs768499336

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67375231_67375238dup , CM000678.2:g.67375231_67375238dup GRCh38
NC_000016.9:g.67409134_67409141dup , CM000678.1:g.67409134_67409141dup GRCh37
NC_000016.8:g.65966635_65966642dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000329956.11:c.1495-16_1495-9dup MANE Select ENSP00000329943.6:n.1495-16_1495-9dup
ENST00000329956.10:c.1495-16_1495-9dup ENSP00000329943.6:n.1495-16_1495-9dup
ENST00000435835.3:c.1132-3358_1132-3351dup ENSP00000411122.3:n.1132-3358_1132-3351dup
ENST00000563189.5:c.1132-16_1132-9dup ENSP00000455103.1:n.1132-16_1132-9dup
ENST00000565019.6:c.1072-84_1072-77dup
ENST00000567723.5:c.*821-16_*821-9dup ENSP00000455799.1:n.*821-16_*821-9dup
ENST00000567823.5:c.215-16_215-9dup ENSP00000456164.1:n.215-16_215-9dup
ENST00000568010.5:c.*246-27_*246-20dup ENSP00000455018.1:n.*246-27_*246-20dup
NM_001161575.1:c.1132-16_1132-9dup NP_001155047.1:n.1132-16_1132-9dup
NM_018296.5:c.1495-16_1495-9dup NP_060766.5:n.1495-16_1495-9dup
XM_005256025.2:c.1495-16_1495-9dup XP_005256082.1:n.1495-16_1495-9dup
XM_005256026.2:c.1054-16_1054-9dup XP_005256083.1:n.1054-16_1054-9dup
XM_005256027.2:c.1495-16_1495-9dup XP_005256084.1:n.1495-16_1495-9dup
XM_005256028.1:c.991-16_991-9dup XP_005256085.1:n.991-16_991-9dup
XM_011523199.1:c.1495-16_1495-9dup XP_011521501.1:n.1495-16_1495-9dup
XM_011523200.1:c.1495-16_1495-9dup XP_011521502.1:n.1495-16_1495-9dup
XM_011523201.1:c.991-16_991-9dup XP_011521503.1:n.991-16_991-9dup
XM_011523202.1:c.988-16_988-9dup XP_011521504.1:n.988-16_988-9dup
XM_011523203.1:c.877-16_877-9dup XP_011521505.1:n.877-16_877-9dup
XM_011523204.1:c.769-16_769-9dup XP_011521506.1:n.769-16_769-9dup
XM_011523205.1:c.769-16_769-9dup XP_011521507.1:n.769-16_769-9dup
XR_243416.2:n.1514-16_1514-9dup
XR_429723.1:n.1514-27_1514-20dup
XM_011523202.2:c.988-16_988-9dup XP_011521504.1:n.988-16_988-9dup
XM_017023400.2:c.1495-16_1495-9dup XP_016878889.1:n.1495-16_1495-9dup
XM_017023401.1:c.755-27_755-20dup XP_016878890.1:n.755-27_755-20dup
XM_017023402.1:c.578-27_578-20dup XP_016878891.1:n.578-27_578-20dup
XM_024450338.1:c.769-16_769-9dup XP_024306106.1:n.769-16_769-9dup
NM_018296.6:c.1495-16_1495-9dup MANE Select NP_060766.5:n.1495-16_1495-9dup
NM_001161575.2:c.1132-16_1132-9dup NP_001155047.1:n.1132-16_1132-9dup