Canonical Allele Identifier: CA3134990127
Gene: LMBRD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.69701470C= , CM000668.2:g.69701470C= GRCh38
NC_000006.11:g.70411362C= , CM000668.1:g.70411362C= GRCh37
NC_000006.10:g.70468083C= NCBI36
NG_016012.1:g.100688G=
NG_016012.2:g.170147G=

Transcript Alleles

HGVS Amino-acid Change
NM_018368.4:c.1056G= MANE Select NP_060838.3:p.Leu352=
ENST00000649934.3:c.1056G= MANE Select ENSP00000497690.1:p.Leu352=
NM_001363722.1:c.837G= NP_001350651.1:p.Leu279=
NM_001363722.2:c.837G= NP_001350651.1:p.Leu279=
NM_001367271.1:c.837G= NP_001354200.1:p.Leu279=
NM_001367272.1:c.837G= NP_001354201.1:p.Leu279=
NM_018368.3:c.1056G= NP_060838.3:p.Leu352=
ENST00000370570.5:c.837G= ENSP00000359602.1:p.Leu279=
ENST00000370570.6:c.837G= ENSP00000359602.1:p.Leu279=
ENST00000370577.7:c.1056G= ENSP00000359609.3:p.Leu352=
ENST00000472827.1:c.1056G= ENSP00000433385.1:p.Leu352=
ENST00000472827.2:c.*221G= ENSP00000433385.2:n.*221G=
ENST00000647650.1:c.*553G= ENSP00000497808.1:n.*553G=
ENST00000647655.1:n.2659G=
ENST00000647934.1:n.1376G=
ENST00000647964.1:c.837G= ENSP00000496784.1:p.Leu279=
ENST00000648168.1:c.837G= ENSP00000498178.1:p.Leu279=
ENST00000648210.1:n.867G=
ENST00000648265.1:n.923G=
ENST00000648303.1:c.*629G= ENSP00000498133.1:n.*629G=
ENST00000648394.1:c.837G= ENSP00000497302.1:p.Leu279=
ENST00000648635.1:c.*821G= ENSP00000497204.1:n.*821G=
ENST00000648743.1:c.837G= ENSP00000497135.1:p.Leu279=
ENST00000649011.1:c.1122G= ENSP00000497575.1:p.Leu374=
ENST00000649028.1:c.837G= ENSP00000498034.1:p.Leu279=
ENST00000649054.1:c.*113G= ENSP00000496991.1:n.*113G=
ENST00000649057.1:c.*621G= ENSP00000497639.1:n.*621G=
ENST00000649166.1:c.*740G= ENSP00000496844.1:n.*740G=
ENST00000649370.1:n.1247G=
ENST00000649673.1:c.*412G= ENSP00000497864.1:n.*412G=
ENST00000649679.1:c.837G= ENSP00000497387.1:p.Leu279=
ENST00000649744.1:n.1244G=
ENST00000649795.1:c.*643G= ENSP00000498147.1:n.*643G=
ENST00000649918.1:c.837G= ENSP00000497487.1:p.Leu279=
ENST00000649958.1:c.*641G= ENSP00000496827.1:n.*641G=
ENST00000650035.1:c.837G= ENSP00000497703.1:p.Leu279=
ENST00000650043.1:n.1035G=
ENST00000650107.1:c.837G= ENSP00000497124.1:p.Leu279=
ENST00000650124.1:c.*566G= ENSP00000497903.1:n.*566G=
ENST00000650473.1:c.809G= ENSP00000497045.1:n.809G=
XM_006715511.2:c.444G= XP_006715574.1:p.Leu148=
XM_011535941.1:c.837G= XP_011534243.1:p.Leu279=
XM_024446488.1:c.837G= XP_024302256.1:p.Leu279=