Canonical Allele Identifier: CA3879675

Gene: LMBRD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.69700809T>C , CM000668.2:g.69700809T>C	GRCh38
NC_000006.11:g.70410701T>C , CM000668.1:g.70410701T>C	GRCh37
NC_000006.10:g.70467422T>C	NCBI36
NG_016012.1:g.101349A>G
NG_016012.2:g.170808A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370570.6:c.925A>G	ENSP00000359602.1:p.Met309Val
ENST00000472827.2:c.*309A>G	ENSP00000433385.2:n.*309A>G
ENST00000647650.1:c.*641A>G	ENSP00000497808.1:n.*641A>G
ENST00000647655.1:n.2747A>G
ENST00000647934.1:n.1464A>G
ENST00000647964.1:c.925A>G	ENSP00000496784.1:p.Met309Val
ENST00000648168.1:c.925A>G	ENSP00000498178.1:p.Met309Val
ENST00000648210.1:n.955A>G
ENST00000648265.1:n.1011A>G
ENST00000648303.1:c.*717A>G	ENSP00000498133.1:n.*717A>G
ENST00000648394.1:c.925A>G	ENSP00000497302.1:p.Met309Val
ENST00000648635.1:c.*909A>G	ENSP00000497204.1:n.*909A>G
ENST00000648743.1:c.925A>G	ENSP00000497135.1:p.Met309Val
ENST00000649011.1:c.1210A>G	ENSP00000497575.1:p.Met404Val
ENST00000649028.1:c.925A>G	ENSP00000498034.1:p.Met309Val
ENST00000649054.1:c.*201A>G	ENSP00000496991.1:n.*201A>G
ENST00000649057.1:c.*709A>G	ENSP00000497639.1:n.*709A>G
ENST00000649166.1:c.*828A>G	ENSP00000496844.1:n.*828A>G
ENST00000649370.1:n.1335A>G
ENST00000649673.1:c.*500A>G	ENSP00000497864.1:n.*500A>G
ENST00000649679.1:c.925A>G	ENSP00000497387.1:p.Met309Val
ENST00000649744.1:n.1332A>G
ENST00000649918.1:c.925A>G	ENSP00000497487.1:p.Met309Val
ENST00000649934.3:c.1144A>G MANE Select	ENSP00000497690.1:p.Met382Val
ENST00000649958.1:c.*729A>G	ENSP00000496827.1:n.*729A>G
ENST00000650035.1:c.925A>G	ENSP00000497703.1:p.Met309Val
ENST00000650043.1:n.1123A>G
ENST00000650107.1:c.925A>G	ENSP00000497124.1:p.Met309Val
ENST00000650124.1:c.*594-7A>G	ENSP00000497903.1:n.*594-7A>G
ENST00000650473.1:c.897A>G	ENSP00000497045.1:n.897A>G
ENST00000370570.5:c.925A>G	ENSP00000359602.1:p.Met309Val
ENST00000370577.7:c.1144A>G	ENSP00000359609.3:p.Met382Val
ENST00000472827.1:c.1084-7A>G	ENSP00000433385.1:n.1084-7A>G
NM_018368.3:c.1144A>G	NP_060838.3:p.Met382Val
XM_006715511.2:c.532A>G	XP_006715574.1:p.Met178Val
XM_011535941.1:c.925A>G	XP_011534243.1:p.Met309Val
NM_001363722.1:c.925A>G	NP_001350651.1:p.Met309Val
XM_024446488.1:c.925A>G	XP_024302256.1:p.Met309Val
NM_001363722.2:c.925A>G	NP_001350651.1:p.Met309Val
NM_001367271.1:c.925A>G	NP_001354200.1:p.Met309Val
NM_001367272.1:c.925A>G	NP_001354201.1:p.Met309Val
NM_018368.4:c.1144A>G MANE Select	NP_060838.3:p.Met382Val