Canonical Allele Identifier: CA3879591

Gene: LMBRD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.69697633T>C , CM000668.2:g.69697633T>C	GRCh38
NC_000006.11:g.70407525T>C , CM000668.1:g.70407525T>C	GRCh37
NC_000006.10:g.70464246T>C	NCBI36
NG_016012.1:g.104525A>G
NG_016012.2:g.173984A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_018368.4:c.1347A>G MANE Select	NP_060838.3:p.Ile449Met
ENST00000649934.3:c.1347A>G MANE Select	ENSP00000497690.1:p.Ile449Met
NM_001363722.1:c.1128A>G	NP_001350651.1:p.Ile376Met
NM_001363722.2:c.1128A>G	NP_001350651.1:p.Ile376Met
NM_001367271.1:c.1128A>G	NP_001354200.1:p.Ile376Met
NM_001367272.1:c.1128A>G	NP_001354201.1:p.Ile376Met
NM_018368.3:c.1347A>G	NP_060838.3:p.Ile449Met
ENST00000370570.5:c.1128A>G	ENSP00000359602.1:p.Ile376Met
ENST00000370570.6:c.1128A>G	ENSP00000359602.1:p.Ile376Met
ENST00000370577.7:c.1347A>G	ENSP00000359609.3:p.Ile449Met
ENST00000472827.1:c.*101A>G	ENSP00000433385.1:n.*101A>G
ENST00000472827.2:c.*512A>G	ENSP00000433385.2:n.*512A>G
ENST00000647650.1:c.*844A>G	ENSP00000497808.1:n.*844A>G
ENST00000647655.1:n.2950A>G
ENST00000647934.1:n.1667A>G
ENST00000647964.1:c.1128A>G	ENSP00000496784.1:p.Ile376Met
ENST00000648168.1:c.1128A>G	ENSP00000498178.1:p.Ile376Met
ENST00000648210.1:n.1158A>G
ENST00000648265.1:n.1214A>G
ENST00000648303.1:c.*920A>G	ENSP00000498133.1:n.*920A>G
ENST00000648394.1:c.1128A>G	ENSP00000497302.1:p.Ile376Met
ENST00000648635.1:c.*1112A>G	ENSP00000497204.1:n.*1112A>G
ENST00000648743.1:c.1128A>G	ENSP00000497135.1:p.Ile376Met
ENST00000649011.1:c.1413A>G	ENSP00000497575.1:p.Ile471Met
ENST00000649028.1:c.1128A>G	ENSP00000498034.1:p.Ile376Met
ENST00000649054.1:c.*404A>G	ENSP00000496991.1:n.*404A>G
ENST00000649057.1:c.*912A>G	ENSP00000497639.1:n.*912A>G
ENST00000649166.1:c.*1031A>G	ENSP00000496844.1:n.*1031A>G
ENST00000649370.1:n.1538A>G
ENST00000649673.1:c.*703A>G	ENSP00000497864.1:n.*703A>G
ENST00000649679.1:c.1128A>G	ENSP00000497387.1:p.Ile376Met
ENST00000649744.1:n.1535A>G
ENST00000649918.1:c.1128A>G	ENSP00000497487.1:p.Ile376Met
ENST00000649958.1:c.*932A>G	ENSP00000496827.1:n.*932A>G
ENST00000650035.1:c.1128A>G	ENSP00000497703.1:p.Ile376Met
ENST00000650043.1:n.1326A>G
ENST00000650107.1:c.1128A>G	ENSP00000497124.1:p.Ile376Met
ENST00000650124.1:c.*790A>G	ENSP00000497903.1:n.*790A>G
ENST00000650473.1:c.1100A>G	ENSP00000497045.1:n.1100A>G
ENST00000651675.1:c.91A>G
XM_006715511.2:c.735A>G	XP_006715574.1:p.Ile245Met
XM_011535941.1:c.1128A>G	XP_011534243.1:p.Ile376Met
XM_024446488.1:c.1128A>G	XP_024302256.1:p.Ile376Met