Canonical Allele Identifier: CA495962213

Gene: LRRC36

Linked Data

• MyVariant Identifiers: chr16:g.67409284C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67375381C>G , CM000678.2:g.67375381C>G	GRCh38
NC_000016.9:g.67409284C>G , CM000678.1:g.67409284C>G	GRCh37
NC_000016.8:g.65966785C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329956.11:c.1629C>G MANE Select	ENSP00000329943.6:p.Ser543=
ENST00000329956.10:c.1629C>G	ENSP00000329943.6:p.Ser543=
ENST00000435835.3:c.1132-3208C>G	ENSP00000411122.3:n.1132-3208C>G
ENST00000563189.5:c.1266C>G	ENSP00000455103.1:p.Ser422=
ENST00000565019.6:c.1138C>G
ENST00000567723.5:c.*955C>G	ENSP00000455799.1:n.*955C>G
ENST00000567823.5:c.*124C>G	ENSP00000456164.1:n.*124C>G
ENST00000568010.5:c.*369C>G	ENSP00000455018.1:n.*369C>G
NM_001161575.1:c.1266C>G	NP_001155047.1:p.Ser422=
NM_018296.5:c.1629C>G	NP_060766.5:p.Ser543=
XM_005256025.2:c.1629C>G	XP_005256082.1:p.Ser543=
XM_005256026.2:c.1188C>G	XP_005256083.1:p.Ser396=
XM_005256027.2:c.1629C>G	XP_005256084.1:p.Ser543=
XM_005256028.1:c.1125C>G	XP_005256085.1:p.Ser375=
XM_011523199.1:c.1629C>G	XP_011521501.1:p.Ser543=
XM_011523200.1:c.1629C>G	XP_011521502.1:p.Ser543=
XM_011523201.1:c.1125C>G	XP_011521503.1:p.Ser375=
XM_011523202.1:c.1122C>G	XP_011521504.1:p.Ser374=
XM_011523203.1:c.1011C>G	XP_011521505.1:p.Ser337=
XM_011523204.1:c.903C>G	XP_011521506.1:p.Ser301=
XM_011523205.1:c.903C>G	XP_011521507.1:p.Ser301=
XR_243416.2:n.1648C>G
XR_429723.1:n.1637C>G
XM_011523202.2:c.1122C>G	XP_011521504.1:p.Ser374=
XM_017023400.2:c.1629C>G	XP_016878889.1:p.Ser543=
XM_017023401.1:c.878C>G	XP_016878890.1:p.Pro293Arg
XM_017023402.1:c.701C>G	XP_016878891.1:p.Pro234Arg
XM_024450338.1:c.903C>G	XP_024306106.1:p.Ser301=
NM_018296.6:c.1629C>G MANE Select	NP_060766.5:p.Ser543=
NM_001161575.2:c.1266C>G	NP_001155047.1:p.Ser422=