Canonical Allele Identifier: CA2229281085

Gene: LRRC36

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67375362A= , CM000678.2:g.67375362A=	GRCh38
NC_000016.9:g.67409265A= , CM000678.1:g.67409265A=	GRCh37
NC_000016.8:g.65966766A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329956.11:c.1610A= MANE Select	ENSP00000329943.6:p.Asp537=
ENST00000329956.10:c.1610A=	ENSP00000329943.6:p.Asp537=
ENST00000435835.3:c.1132-3227A=	ENSP00000411122.3:n.1132-3227A=
ENST00000563189.5:c.1247A=	ENSP00000455103.1:p.Asp416=
ENST00000565019.6:c.1119A=
ENST00000567723.5:c.*936A=	ENSP00000455799.1:n.*936A=
ENST00000567823.5:c.*105A=	ENSP00000456164.1:n.*105A=
ENST00000568010.5:c.*350A=	ENSP00000455018.1:n.*350A=
NM_001161575.1:c.1247A=	NP_001155047.1:p.Asp416=
NM_018296.5:c.1610A=	NP_060766.5:p.Asp537=
XM_005256025.2:c.1610A=	XP_005256082.1:p.Asp537=
XM_005256026.2:c.1169A=	XP_005256083.1:p.Asp390=
XM_005256027.2:c.1610A=	XP_005256084.1:p.Asp537=
XM_005256028.1:c.1106A=	XP_005256085.1:p.Asp369=
XM_011523199.1:c.1610A=	XP_011521501.1:p.Asp537=
XM_011523200.1:c.1610A=	XP_011521502.1:p.Asp537=
XM_011523201.1:c.1106A=	XP_011521503.1:p.Asp369=
XM_011523202.1:c.1103A=	XP_011521504.1:p.Asp368=
XM_011523203.1:c.992A=	XP_011521505.1:p.Asp331=
XM_011523204.1:c.884A=	XP_011521506.1:p.Asp295=
XM_011523205.1:c.884A=	XP_011521507.1:p.Asp295=
XR_243416.2:n.1629A=
XR_429723.1:n.1618A=
XM_011523202.2:c.1103A=	XP_011521504.1:p.Asp368=
XM_017023400.2:c.1610A=	XP_016878889.1:p.Asp537=
XM_017023401.1:c.859A=	XP_016878890.1:p.Ile287=
XM_017023402.1:c.682A=	XP_016878891.1:p.Ile228=
XM_024450338.1:c.884A=	XP_024306106.1:p.Asp295=
NM_018296.6:c.1610A= MANE Select	NP_060766.5:p.Asp537=
NM_001161575.2:c.1247A=	NP_001155047.1:p.Asp416=