Canonical Allele Identifier: CA396267968

Gene: LRRC36

Linked Data

• MyVariant Identifiers: chr16:g.67409179C>G (hg19) ; chr16:g.67375276C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67375276C>G , CM000678.2:g.67375276C>G	GRCh38
NC_000016.9:g.67409179C>G , CM000678.1:g.67409179C>G	GRCh37
NC_000016.8:g.65966680C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329956.11:c.1524C>G MANE Select	ENSP00000329943.6:p.His508Gln
ENST00000329956.10:c.1524C>G	ENSP00000329943.6:p.His508Gln
ENST00000435835.3:c.1132-3313C>G	ENSP00000411122.3:n.1132-3313C>G
ENST00000563189.5:c.1161C>G	ENSP00000455103.1:p.His387Gln
ENST00000565019.6:c.1072-39C>G
ENST00000567723.5:c.*850C>G	ENSP00000455799.1:n.*850C>G
ENST00000567823.5:c.*19C>G	ENSP00000456164.1:n.*19C>G
ENST00000568010.5:c.*264C>G	ENSP00000455018.1:n.*264C>G
NM_001161575.1:c.1161C>G	NP_001155047.1:p.His387Gln
NM_018296.5:c.1524C>G	NP_060766.5:p.His508Gln
XM_005256025.2:c.1524C>G	XP_005256082.1:p.His508Gln
XM_005256026.2:c.1083C>G	XP_005256083.1:p.His361Gln
XM_005256027.2:c.1524C>G	XP_005256084.1:p.His508Gln
XM_005256028.1:c.1020C>G	XP_005256085.1:p.His340Gln
XM_011523199.1:c.1524C>G	XP_011521501.1:p.His508Gln
XM_011523200.1:c.1524C>G	XP_011521502.1:p.His508Gln
XM_011523201.1:c.1020C>G	XP_011521503.1:p.His340Gln
XM_011523202.1:c.1017C>G	XP_011521504.1:p.His339Gln
XM_011523203.1:c.906C>G	XP_011521505.1:p.His302Gln
XM_011523204.1:c.798C>G	XP_011521506.1:p.His266Gln
XM_011523205.1:c.798C>G	XP_011521507.1:p.His266Gln
XR_243416.2:n.1543C>G
XR_429723.1:n.1532C>G
XM_011523202.2:c.1017C>G	XP_011521504.1:p.His339Gln
XM_017023400.2:c.1524C>G	XP_016878889.1:p.His508Gln
XM_017023401.1:c.773C>G	XP_016878890.1:p.Thr258Arg
XM_017023402.1:c.596C>G	XP_016878891.1:p.Thr199Arg
XM_024450338.1:c.798C>G	XP_024306106.1:p.His266Gln
NM_018296.6:c.1524C>G MANE Select	NP_060766.5:p.His508Gln
NM_001161575.2:c.1161C>G	NP_001155047.1:p.His387Gln