Canonical Allele Identifier: CA450707996

Gene: LMBRD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.69697612G>T , CM000668.2:g.69697612G>T	GRCh38
NC_000006.11:g.70407504G>T , CM000668.1:g.70407504G>T	GRCh37
NC_000006.10:g.70464225G>T	NCBI36
NG_016012.1:g.104546C>A
NG_016012.2:g.174005C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_018368.4:c.1368C>A MANE Select	NP_060838.3:p.Gly456=
ENST00000649934.3:c.1368C>A MANE Select	ENSP00000497690.1:p.Gly456=
NM_001363722.1:c.1149C>A	NP_001350651.1:p.Gly383=
NM_001363722.2:c.1149C>A	NP_001350651.1:p.Gly383=
NM_001367271.1:c.1149C>A	NP_001354200.1:p.Gly383=
NM_001367272.1:c.1149C>A	NP_001354201.1:p.Gly383=
NM_018368.3:c.1368C>A	NP_060838.3:p.Gly456=
ENST00000370570.5:c.1149C>A	ENSP00000359602.1:p.Gly383=
ENST00000370570.6:c.1149C>A	ENSP00000359602.1:p.Gly383=
ENST00000370577.7:c.1368C>A	ENSP00000359609.3:p.Gly456=
ENST00000472827.1:c.*122C>A	ENSP00000433385.1:n.*122C>A
ENST00000472827.2:c.*533C>A	ENSP00000433385.2:n.*533C>A
ENST00000647650.1:c.*865C>A	ENSP00000497808.1:n.*865C>A
ENST00000647655.1:n.2971C>A
ENST00000647934.1:n.1688C>A
ENST00000647964.1:c.1149C>A	ENSP00000496784.1:p.Gly383=
ENST00000648168.1:c.1149C>A	ENSP00000498178.1:p.Gly383=
ENST00000648210.1:n.1179C>A
ENST00000648265.1:n.1235C>A
ENST00000648303.1:c.*941C>A	ENSP00000498133.1:n.*941C>A
ENST00000648394.1:c.1149C>A	ENSP00000497302.1:p.Gly383=
ENST00000648635.1:c.*1133C>A	ENSP00000497204.1:n.*1133C>A
ENST00000648743.1:c.1149C>A	ENSP00000497135.1:p.Gly383=
ENST00000649011.1:c.1434C>A	ENSP00000497575.1:p.Gly478=
ENST00000649028.1:c.1149C>A	ENSP00000498034.1:p.Gly383=
ENST00000649054.1:c.*425C>A	ENSP00000496991.1:n.*425C>A
ENST00000649057.1:c.*933C>A	ENSP00000497639.1:n.*933C>A
ENST00000649166.1:c.*1052C>A	ENSP00000496844.1:n.*1052C>A
ENST00000649370.1:n.1559C>A
ENST00000649673.1:c.*724C>A	ENSP00000497864.1:n.*724C>A
ENST00000649679.1:c.1149C>A	ENSP00000497387.1:p.Gly383=
ENST00000649744.1:n.1556C>A
ENST00000649918.1:c.1149C>A	ENSP00000497487.1:p.Gly383=
ENST00000649958.1:c.*953C>A	ENSP00000496827.1:n.*953C>A
ENST00000650035.1:c.1149C>A	ENSP00000497703.1:p.Gly383=
ENST00000650043.1:n.1347C>A
ENST00000650107.1:c.1149C>A	ENSP00000497124.1:p.Gly383=
ENST00000650124.1:c.*811C>A	ENSP00000497903.1:n.*811C>A
ENST00000650473.1:c.1121C>A	ENSP00000497045.1:n.1121C>A
ENST00000651675.1:c.112C>A
XM_006715511.2:c.756C>A	XP_006715574.1:p.Gly252=
XM_011535941.1:c.1149C>A	XP_011534243.1:p.Gly383=
XM_024446488.1:c.1149C>A	XP_024302256.1:p.Gly383=