Canonical Allele Identifier: CA140850698

Gene: LMBRD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.69676168T>C , CM000668.2:g.69676168T>C	GRCh38
NC_000006.11:g.70386060T>C , CM000668.1:g.70386060T>C	GRCh37
NC_000006.10:g.70442781T>C	NCBI36
NG_016012.1:g.125990A>G
NG_016012.2:g.195449A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370570.6:c.1394A>G	ENSP00000359602.1:p.Tyr465Cys
ENST00000472827.2:c.*778A>G	ENSP00000433385.2:n.*778A>G
ENST00000647650.1:c.*1110A>G	ENSP00000497808.1:n.*1110A>G
ENST00000647655.1:n.3216A>G
ENST00000647934.1:n.1933A>G
ENST00000647964.1:c.1394A>G	ENSP00000496784.1:p.Tyr465Cys
ENST00000648168.1:c.1394A>G	ENSP00000498178.1:p.Tyr465Cys
ENST00000648210.1:n.1424A>G
ENST00000648265.1:n.1480A>G
ENST00000648303.1:c.*1186A>G	ENSP00000498133.1:n.*1186A>G
ENST00000648394.1:c.1394A>G	ENSP00000497302.1:p.Tyr465Cys
ENST00000648635.1:c.*1378A>G	ENSP00000497204.1:n.*1378A>G
ENST00000648743.1:c.1394A>G	ENSP00000497135.1:p.Tyr465Cys
ENST00000649011.1:c.1679A>G	ENSP00000497575.1:p.Tyr560Cys
ENST00000649028.1:c.1394A>G	ENSP00000498034.1:p.Tyr465Cys
ENST00000649054.1:c.*670A>G	ENSP00000496991.1:n.*670A>G
ENST00000649057.1:c.*1178A>G	ENSP00000497639.1:n.*1178A>G
ENST00000649166.1:c.*1297A>G	ENSP00000496844.1:n.*1297A>G
ENST00000649370.1:n.1804A>G
ENST00000649673.1:c.*969A>G	ENSP00000497864.1:n.*969A>G
ENST00000649679.1:c.1394A>G	ENSP00000497387.1:p.Tyr465Cys
ENST00000649744.1:n.1801A>G
ENST00000649918.1:c.1394A>G	ENSP00000497487.1:p.Tyr465Cys
ENST00000649934.3:c.1613A>G MANE Select	ENSP00000497690.1:p.Tyr538Cys
ENST00000649958.1:c.*1198A>G	ENSP00000496827.1:n.*1198A>G
ENST00000650035.1:c.1394A>G	ENSP00000497703.1:p.Tyr465Cys
ENST00000650043.1:n.1592A>G
ENST00000650107.1:c.1394A>G	ENSP00000497124.1:p.Tyr465Cys
ENST00000650124.1:c.*1056A>G	ENSP00000497903.1:n.*1056A>G
ENST00000650473.1:c.1366A>G	ENSP00000497045.1:n.1366A>G
ENST00000651675.1:c.357A>G
ENST00000370570.5:c.1394A>G	ENSP00000359602.1:p.Tyr465Cys
ENST00000370577.7:c.1613A>G	ENSP00000359609.3:p.Tyr538Cys
ENST00000472827.1:c.*367A>G	ENSP00000433385.1:n.*367A>G
NM_018368.3:c.1613A>G	NP_060838.3:p.Tyr538Cys
XM_006715511.2:c.1001A>G	XP_006715574.1:p.Tyr334Cys
XM_011535941.1:c.1394A>G	XP_011534243.1:p.Tyr465Cys
NM_001363722.1:c.1394A>G	NP_001350651.1:p.Tyr465Cys
XM_024446488.1:c.1394A>G	XP_024302256.1:p.Tyr465Cys
NM_001363722.2:c.1394A>G	NP_001350651.1:p.Tyr465Cys
NM_001367271.1:c.1394A>G	NP_001354200.1:p.Tyr465Cys
NM_001367272.1:c.1394A>G	NP_001354201.1:p.Tyr465Cys
NM_018368.4:c.1613A>G MANE Select	NP_060838.3:p.Tyr538Cys