Canonical Allele Identifier: CA2229281091

Gene: LRRC36

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67375379T= , CM000678.2:g.67375379T=	GRCh38
NC_000016.9:g.67409282T= , CM000678.1:g.67409282T=	GRCh37
NC_000016.8:g.65966783T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329956.11:c.1627T= MANE Select	ENSP00000329943.6:p.Ser543=
ENST00000329956.10:c.1627T=	ENSP00000329943.6:p.Ser543=
ENST00000435835.3:c.1132-3210T=	ENSP00000411122.3:n.1132-3210T=
ENST00000563189.5:c.1264T=	ENSP00000455103.1:p.Ser422=
ENST00000565019.6:c.1136T=
ENST00000567723.5:c.*953T=	ENSP00000455799.1:n.*953T=
ENST00000567823.5:c.*122T=	ENSP00000456164.1:n.*122T=
ENST00000568010.5:c.*367T=	ENSP00000455018.1:n.*367T=
NM_001161575.1:c.1264T=	NP_001155047.1:p.Ser422=
NM_018296.5:c.1627T=	NP_060766.5:p.Ser543=
XM_005256025.2:c.1627T=	XP_005256082.1:p.Ser543=
XM_005256026.2:c.1186T=	XP_005256083.1:p.Ser396=
XM_005256027.2:c.1627T=	XP_005256084.1:p.Ser543=
XM_005256028.1:c.1123T=	XP_005256085.1:p.Ser375=
XM_011523199.1:c.1627T=	XP_011521501.1:p.Ser543=
XM_011523200.1:c.1627T=	XP_011521502.1:p.Ser543=
XM_011523201.1:c.1123T=	XP_011521503.1:p.Ser375=
XM_011523202.1:c.1120T=	XP_011521504.1:p.Ser374=
XM_011523203.1:c.1009T=	XP_011521505.1:p.Ser337=
XM_011523204.1:c.901T=	XP_011521506.1:p.Ser301=
XM_011523205.1:c.901T=	XP_011521507.1:p.Ser301=
XR_243416.2:n.1646T=
XR_429723.1:n.1635T=
XM_011523202.2:c.1120T=	XP_011521504.1:p.Ser374=
XM_017023400.2:c.1627T=	XP_016878889.1:p.Ser543=
XM_017023401.1:c.876T=	XP_016878890.1:p.Ala292=
XM_017023402.1:c.699T=	XP_016878891.1:p.Ala233=
XM_024450338.1:c.901T=	XP_024306106.1:p.Ser301=
NM_018296.6:c.1627T= MANE Select	NP_060766.5:p.Ser543=
NM_001161575.2:c.1264T=	NP_001155047.1:p.Ser422=