Canonical Allele Identifier: CA2229281023

Gene: LRRC36

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67375207T= , CM000678.2:g.67375207T=	GRCh38
NC_000016.9:g.67409110T= , CM000678.1:g.67409110T=	GRCh37
NC_000016.8:g.65966611T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329956.11:c.1495-40T= MANE Select	ENSP00000329943.6:n.1495-40T=
ENST00000329956.10:c.1495-40T=	ENSP00000329943.6:n.1495-40T=
ENST00000435835.3:c.1132-3382T=	ENSP00000411122.3:n.1132-3382T=
ENST00000563189.5:c.1132-40T=	ENSP00000455103.1:n.1132-40T=
ENST00000565019.6:c.1072-108T=
ENST00000567723.5:c.*821-40T=	ENSP00000455799.1:n.*821-40T=
ENST00000567823.5:c.215-40T=	ENSP00000456164.1:n.215-40T=
ENST00000568010.5:c.*246-51T=	ENSP00000455018.1:n.*246-51T=
NM_001161575.1:c.1132-40T=	NP_001155047.1:n.1132-40T=
NM_018296.5:c.1495-40T=	NP_060766.5:n.1495-40T=
XM_005256025.2:c.1495-40T=	XP_005256082.1:n.1495-40T=
XM_005256026.2:c.1054-40T=	XP_005256083.1:n.1054-40T=
XM_005256027.2:c.1495-40T=	XP_005256084.1:n.1495-40T=
XM_005256028.1:c.991-40T=	XP_005256085.1:n.991-40T=
XM_011523199.1:c.1495-40T=	XP_011521501.1:n.1495-40T=
XM_011523200.1:c.1495-40T=	XP_011521502.1:n.1495-40T=
XM_011523201.1:c.991-40T=	XP_011521503.1:n.991-40T=
XM_011523202.1:c.988-40T=	XP_011521504.1:n.988-40T=
XM_011523203.1:c.877-40T=	XP_011521505.1:n.877-40T=
XM_011523204.1:c.769-40T=	XP_011521506.1:n.769-40T=
XM_011523205.1:c.769-40T=	XP_011521507.1:n.769-40T=
XR_243416.2:n.1514-40T=
XR_429723.1:n.1514-51T=
XM_011523202.2:c.988-40T=	XP_011521504.1:n.988-40T=
XM_017023400.2:c.1495-40T=	XP_016878889.1:n.1495-40T=
XM_017023401.1:c.755-51T=	XP_016878890.1:n.755-51T=
XM_017023402.1:c.578-51T=	XP_016878891.1:n.578-51T=
XM_024450338.1:c.769-40T=	XP_024306106.1:n.769-40T=
NM_018296.6:c.1495-40T= MANE Select	NP_060766.5:n.1495-40T=
NM_001161575.2:c.1132-40T=	NP_001155047.1:n.1132-40T=