Canonical Allele Identifier: CA1139770167

Gene: LRRC36

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67375296_67375297insGGGGGGGGGGGGGGGGGGGGGGG , CM000678.2:g.67375296_67375297insGGGGGGGGGGGGGGGGGGGGGGG	GRCh38
NC_000016.9:g.67409199_67409200insGGGGGGGGGGGGGGGGGGGGGGG , CM000678.1:g.67409199_67409200insGGGGGGGGGGGGGGGGGGGGGGG	GRCh37
NC_000016.8:g.65966700_65966701insGGGGGGGGGGGGGGGGGGGGGGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329956.11:c.1544_1545insGGGGGGGGGGGGGGGGGGGGGGG MANE Select	ENSP00000329943.6:p.Ser515ArgfsTer?
ENST00000329956.10:c.1544_1545insGGGGGGGGGGGGGGGGGGGGGGG	ENSP00000329943.6:p.Ser515ArgfsTer?
ENST00000435835.3:c.1132-3293_1132-3292insGGGGGGGGGGGGGGGGGGGGGGG	ENSP00000411122.3:n.1132-3293_1132-3292insGGGGGGGGGGGGGGGGGGG...
ENST00000563189.5:c.1181_1182insGGGGGGGGGGGGGGGGGGGGGGG	ENSP00000455103.1:p.Ser394ArgfsTer?
ENST00000565019.6:c.1072-19_1072-18insGGGGGGGGGGGGGGGGGGGGGGG
ENST00000567723.5:c.*870_*871insGGGGGGGGGGGGGGGGGGGGGGG	ENSP00000455799.1:n.*870_*871insGGGGGGGGGGGGGGGGGGGGGGG
ENST00000567823.5:c.*39_*40insGGGGGGGGGGGGGGGGGGGGGGG	ENSP00000456164.1:n.*39_*40insGGGGGGGGGGGGGGGGGGGGGGG
ENST00000568010.5:c.*284_*285insGGGGGGGGGGGGGGGGGGGGGGG	ENSP00000455018.1:n.*284_*285insGGGGGGGGGGGGGGGGGGGGGGG
NM_001161575.1:c.1181_1182insGGGGGGGGGGGGGGGGGGGGGGG	NP_001155047.1:p.Ser394ArgfsTer?
NM_018296.5:c.1544_1545insGGGGGGGGGGGGGGGGGGGGGGG	NP_060766.5:p.Ser515ArgfsTer?
XM_005256025.2:c.1544_1545insGGGGGGGGGGGGGGGGGGGGGGG	XP_005256082.1:p.Ser515ArgfsTer?
XM_005256026.2:c.1103_1104insGGGGGGGGGGGGGGGGGGGGGGG	XP_005256083.1:p.Ser368ArgfsTer?
XM_005256027.2:c.1544_1545insGGGGGGGGGGGGGGGGGGGGGGG	XP_005256084.1:p.Ser515ArgfsTer?
XM_005256028.1:c.1040_1041insGGGGGGGGGGGGGGGGGGGGGGG	XP_005256085.1:p.Ser347ArgfsTer?
XM_011523199.1:c.1544_1545insGGGGGGGGGGGGGGGGGGGGGGG	XP_011521501.1:p.Ser515ArgfsTer?
XM_011523200.1:c.1544_1545insGGGGGGGGGGGGGGGGGGGGGGG	XP_011521502.1:p.Ser515ArgfsTer?
XM_011523201.1:c.1040_1041insGGGGGGGGGGGGGGGGGGGGGGG	XP_011521503.1:p.Ser347ArgfsTer?
XM_011523202.1:c.1037_1038insGGGGGGGGGGGGGGGGGGGGGGG	XP_011521504.1:p.Ser346ArgfsTer?
XM_011523203.1:c.926_927insGGGGGGGGGGGGGGGGGGGGGGG	XP_011521505.1:p.Ser309ArgfsTer?
XM_011523204.1:c.818_819insGGGGGGGGGGGGGGGGGGGGGGG	XP_011521506.1:p.Ser273ArgfsTer?
XM_011523205.1:c.818_819insGGGGGGGGGGGGGGGGGGGGGGG	XP_011521507.1:p.Ser273ArgfsTer?
XR_243416.2:n.1563_1564insGGGGGGGGGGGGGGGGGGGGGGG
XR_429723.1:n.1552_1553insGGGGGGGGGGGGGGGGGGGGGGG
XM_011523202.2:c.1037_1038insGGGGGGGGGGGGGGGGGGGGGGG	XP_011521504.1:p.Ser346ArgfsTer?
XM_017023400.2:c.1544_1545insGGGGGGGGGGGGGGGGGGGGGGG	XP_016878889.1:p.Ser515ArgfsTer?
XM_017023401.1:c.793_794insGGGGGGGGGGGGGGGGGGGGGGG	XP_016878890.1:p.Val265GlyfsTer31
XM_017023402.1:c.616_617insGGGGGGGGGGGGGGGGGGGGGGG	XP_016878891.1:p.Val206GlyfsTer31
XM_024450338.1:c.818_819insGGGGGGGGGGGGGGGGGGGGGGG	XP_024306106.1:p.Ser273ArgfsTer?
NM_018296.6:c.1544_1545insGGGGGGGGGGGGGGGGGGGGGGG MANE Select	NP_060766.5:p.Ser515ArgfsTer?
NM_001161575.2:c.1181_1182insGGGGGGGGGGGGGGGGGGGGGGG	NP_001155047.1:p.Ser394ArgfsTer?