Canonical Allele Identifier: CA2229281051

Gene: LRRC36

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67375277G= , CM000678.2:g.67375277G=	GRCh38
NC_000016.9:g.67409180G= , CM000678.1:g.67409180G=	GRCh37
NC_000016.8:g.65966681G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_018296.6:c.1525G= MANE Select	NP_060766.5:p.Gly509=
ENST00000329956.11:c.1525G= MANE Select	ENSP00000329943.6:p.Gly509=
NM_001161575.1:c.1162G=	NP_001155047.1:p.Gly388=
NM_001161575.2:c.1162G=	NP_001155047.1:p.Gly388=
NM_018296.5:c.1525G=	NP_060766.5:p.Gly509=
ENST00000329956.10:c.1525G=	ENSP00000329943.6:p.Gly509=
ENST00000435835.3:c.1132-3312G=	ENSP00000411122.3:n.1132-3312G=
ENST00000563189.5:c.1162G=	ENSP00000455103.1:p.Gly388=
ENST00000565019.6:c.1072-38G=
ENST00000567723.5:c.*851G=	ENSP00000455799.1:n.*851G=
ENST00000567823.5:c.*20G=	ENSP00000456164.1:n.*20G=
ENST00000568010.5:c.*265G=	ENSP00000455018.1:n.*265G=
XM_005256025.2:c.1525G=	XP_005256082.1:p.Gly509=
XM_005256026.2:c.1084G=	XP_005256083.1:p.Gly362=
XM_005256027.2:c.1525G=	XP_005256084.1:p.Gly509=
XM_005256028.1:c.1021G=	XP_005256085.1:p.Gly341=
XM_011523199.1:c.1525G=	XP_011521501.1:p.Gly509=
XM_011523200.1:c.1525G=	XP_011521502.1:p.Gly509=
XM_011523201.1:c.1021G=	XP_011521503.1:p.Gly341=
XM_011523202.1:c.1018G=	XP_011521504.1:p.Gly340=
XM_011523202.2:c.1018G=	XP_011521504.1:p.Gly340=
XM_011523203.1:c.907G=	XP_011521505.1:p.Gly303=
XM_011523204.1:c.799G=	XP_011521506.1:p.Gly267=
XM_011523205.1:c.799G=	XP_011521507.1:p.Gly267=
XM_017023400.2:c.1525G=	XP_016878889.1:p.Gly509=
XM_017023401.1:c.774G=	XP_016878890.1:p.Thr258=
XM_017023402.1:c.597G=	XP_016878891.1:p.Thr199=
XM_024450338.1:c.799G=	XP_024306106.1:p.Gly267=
XR_243416.2:n.1544G=
XR_429723.1:n.1533G=