Canonical Allele Identifier: CA396267752

Gene: LRRC36

Linked Data

• MyVariant Identifiers: chr16:g.67409153C>A (hg19) ; chr16:g.67375250C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67375250C>A , CM000678.2:g.67375250C>A	GRCh38
NC_000016.9:g.67409153C>A , CM000678.1:g.67409153C>A	GRCh37
NC_000016.8:g.65966654C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329956.11:c.1498C>A MANE Select	ENSP00000329943.6:p.Leu500Ile
ENST00000329956.10:c.1498C>A	ENSP00000329943.6:p.Leu500Ile
ENST00000435835.3:c.1132-3339C>A	ENSP00000411122.3:n.1132-3339C>A
ENST00000563189.5:c.1135C>A	ENSP00000455103.1:p.Leu379Ile
ENST00000565019.6:c.1072-65C>A
ENST00000567723.5:c.*824C>A	ENSP00000455799.1:n.*824C>A
ENST00000567823.5:c.218C>A	ENSP00000456164.1:p.Ser73Tyr
ENST00000568010.5:c.*246-8C>A	ENSP00000455018.1:n.*246-8C>A
NM_001161575.1:c.1135C>A	NP_001155047.1:p.Leu379Ile
NM_018296.5:c.1498C>A	NP_060766.5:p.Leu500Ile
XM_005256025.2:c.1498C>A	XP_005256082.1:p.Leu500Ile
XM_005256026.2:c.1057C>A	XP_005256083.1:p.Leu353Ile
XM_005256027.2:c.1498C>A	XP_005256084.1:p.Leu500Ile
XM_005256028.1:c.994C>A	XP_005256085.1:p.Leu332Ile
XM_011523199.1:c.1498C>A	XP_011521501.1:p.Leu500Ile
XM_011523200.1:c.1498C>A	XP_011521502.1:p.Leu500Ile
XM_011523201.1:c.994C>A	XP_011521503.1:p.Leu332Ile
XM_011523202.1:c.991C>A	XP_011521504.1:p.Leu331Ile
XM_011523203.1:c.880C>A	XP_011521505.1:p.Leu294Ile
XM_011523204.1:c.772C>A	XP_011521506.1:p.Leu258Ile
XM_011523205.1:c.772C>A	XP_011521507.1:p.Leu258Ile
XR_243416.2:n.1517C>A
XR_429723.1:n.1514-8C>A
XM_011523202.2:c.991C>A	XP_011521504.1:p.Leu331Ile
XM_017023400.2:c.1498C>A	XP_016878889.1:p.Leu500Ile
XM_017023401.1:c.755-8C>A	XP_016878890.1:n.755-8C>A
XM_017023402.1:c.578-8C>A	XP_016878891.1:n.578-8C>A
XM_024450338.1:c.772C>A	XP_024306106.1:p.Leu258Ile
NM_018296.6:c.1498C>A MANE Select	NP_060766.5:p.Leu500Ile
NM_001161575.2:c.1135C>A	NP_001155047.1:p.Leu379Ile