Canonical Allele Identifier: CA396267776

Gene: LRRC36

Linked Data

• MyVariant Identifiers: chr16:g.67409156T>G (hg19) ; chr16:g.67375253T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67375253T>G , CM000678.2:g.67375253T>G	GRCh38
NC_000016.9:g.67409156T>G , CM000678.1:g.67409156T>G	GRCh37
NC_000016.8:g.65966657T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329956.11:c.1501T>G MANE Select	ENSP00000329943.6:p.Ser501Ala
ENST00000329956.10:c.1501T>G	ENSP00000329943.6:p.Ser501Ala
ENST00000435835.3:c.1132-3336T>G	ENSP00000411122.3:n.1132-3336T>G
ENST00000563189.5:c.1138T>G	ENSP00000455103.1:p.Ser380Ala
ENST00000565019.6:c.1072-62T>G
ENST00000567723.5:c.*827T>G	ENSP00000455799.1:n.*827T>G
ENST00000567823.5:c.221T>G	ENSP00000456164.1:p.Leu74Arg
ENST00000568010.5:c.*246-5T>G	ENSP00000455018.1:n.*246-5T>G
NM_001161575.1:c.1138T>G	NP_001155047.1:p.Ser380Ala
NM_018296.5:c.1501T>G	NP_060766.5:p.Ser501Ala
XM_005256025.2:c.1501T>G	XP_005256082.1:p.Ser501Ala
XM_005256026.2:c.1060T>G	XP_005256083.1:p.Ser354Ala
XM_005256027.2:c.1501T>G	XP_005256084.1:p.Ser501Ala
XM_005256028.1:c.997T>G	XP_005256085.1:p.Ser333Ala
XM_011523199.1:c.1501T>G	XP_011521501.1:p.Ser501Ala
XM_011523200.1:c.1501T>G	XP_011521502.1:p.Ser501Ala
XM_011523201.1:c.997T>G	XP_011521503.1:p.Ser333Ala
XM_011523202.1:c.994T>G	XP_011521504.1:p.Ser332Ala
XM_011523203.1:c.883T>G	XP_011521505.1:p.Ser295Ala
XM_011523204.1:c.775T>G	XP_011521506.1:p.Ser259Ala
XM_011523205.1:c.775T>G	XP_011521507.1:p.Ser259Ala
XR_243416.2:n.1520T>G
XR_429723.1:n.1514-5T>G
XM_011523202.2:c.994T>G	XP_011521504.1:p.Ser332Ala
XM_017023400.2:c.1501T>G	XP_016878889.1:p.Ser501Ala
XM_017023401.1:c.755-5T>G	XP_016878890.1:n.755-5T>G
XM_017023402.1:c.578-5T>G	XP_016878891.1:n.578-5T>G
XM_024450338.1:c.775T>G	XP_024306106.1:p.Ser259Ala
NM_018296.6:c.1501T>G MANE Select	NP_060766.5:p.Ser501Ala
NM_001161575.2:c.1138T>G	NP_001155047.1:p.Ser380Ala