Canonical Allele Identifier: CA396267898

Gene: LRRC36

Linked Data

• MyVariant Identifiers: chr16:g.67409174T>G (hg19) ; chr16:g.67375271T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67375271T>G , CM000678.2:g.67375271T>G	GRCh38
NC_000016.9:g.67409174T>G , CM000678.1:g.67409174T>G	GRCh37
NC_000016.8:g.65966675T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329956.11:c.1519T>G MANE Select	ENSP00000329943.6:p.Leu507Val
ENST00000329956.10:c.1519T>G	ENSP00000329943.6:p.Leu507Val
ENST00000435835.3:c.1132-3318T>G	ENSP00000411122.3:n.1132-3318T>G
ENST00000563189.5:c.1156T>G	ENSP00000455103.1:p.Leu386Val
ENST00000565019.6:c.1072-44T>G
ENST00000567723.5:c.*845T>G	ENSP00000455799.1:n.*845T>G
ENST00000567823.5:c.*14T>G	ENSP00000456164.1:n.*14T>G
ENST00000568010.5:c.*259T>G	ENSP00000455018.1:n.*259T>G
NM_001161575.1:c.1156T>G	NP_001155047.1:p.Leu386Val
NM_018296.5:c.1519T>G	NP_060766.5:p.Leu507Val
XM_005256025.2:c.1519T>G	XP_005256082.1:p.Leu507Val
XM_005256026.2:c.1078T>G	XP_005256083.1:p.Leu360Val
XM_005256027.2:c.1519T>G	XP_005256084.1:p.Leu507Val
XM_005256028.1:c.1015T>G	XP_005256085.1:p.Leu339Val
XM_011523199.1:c.1519T>G	XP_011521501.1:p.Leu507Val
XM_011523200.1:c.1519T>G	XP_011521502.1:p.Leu507Val
XM_011523201.1:c.1015T>G	XP_011521503.1:p.Leu339Val
XM_011523202.1:c.1012T>G	XP_011521504.1:p.Leu338Val
XM_011523203.1:c.901T>G	XP_011521505.1:p.Leu301Val
XM_011523204.1:c.793T>G	XP_011521506.1:p.Leu265Val
XM_011523205.1:c.793T>G	XP_011521507.1:p.Leu265Val
XR_243416.2:n.1538T>G
XR_429723.1:n.1527T>G
XM_011523202.2:c.1012T>G	XP_011521504.1:p.Leu338Val
XM_017023400.2:c.1519T>G	XP_016878889.1:p.Leu507Val
XM_017023401.1:c.768T>G	XP_016878890.1:p.Val256=
XM_017023402.1:c.591T>G	XP_016878891.1:p.Val197=
XM_024450338.1:c.793T>G	XP_024306106.1:p.Leu265Val
NM_018296.6:c.1519T>G MANE Select	NP_060766.5:p.Leu507Val
NM_001161575.2:c.1156T>G	NP_001155047.1:p.Leu386Val