Canonical Allele Identifier: CA3879865

Gene: LMBRD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.69741788C>A , CM000668.2:g.69741788C>A	GRCh38
NC_000006.11:g.70451680C>A , CM000668.1:g.70451680C>A	GRCh37
NC_000006.10:g.70508401C>A	NCBI36
NG_016012.1:g.60370G>T
NG_016012.2:g.129829G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_018368.4:c.562+1G>T MANE Select	NP_060838.3:n.562+1G>T
ENST00000649934.3:c.562+1G>T MANE Select	ENSP00000497690.1:n.562+1G>T
NM_001363722.1:c.343+1G>T	NP_001350651.1:n.343+1G>T
NM_001363722.2:c.343+1G>T	NP_001350651.1:n.343+1G>T
NM_001367271.1:c.343+1G>T	NP_001354200.1:n.343+1G>T
NM_001367272.1:c.343+1G>T	NP_001354201.1:n.343+1G>T
NM_018368.3:c.562+1G>T	NP_060838.3:n.562+1G>T
ENST00000370570.5:c.343+1G>T	ENSP00000359602.1:n.343+1G>T
ENST00000370570.6:c.343+1G>T	ENSP00000359602.1:n.343+1G>T
ENST00000370577.7:c.562+1G>T	ENSP00000359609.3:n.562+1G>T
ENST00000472827.1:c.562+1G>T	ENSP00000433385.1:n.562+1G>T
ENST00000472827.2:c.562+1G>T	ENSP00000433385.2:n.562+1G>T
ENST00000647650.1:c.*59+1G>T	ENSP00000497808.1:n.*59+1G>T
ENST00000647655.1:n.2165+1G>T
ENST00000647934.1:n.882+1G>T
ENST00000647964.1:c.343+1G>T	ENSP00000496784.1:n.343+1G>T
ENST00000648168.1:c.343+1G>T	ENSP00000498178.1:n.343+1G>T
ENST00000648210.1:n.373+1G>T
ENST00000648265.1:n.429+1G>T
ENST00000648303.1:c.*135+1G>T	ENSP00000498133.1:n.*135+1G>T
ENST00000648394.1:c.343+1G>T	ENSP00000497302.1:n.343+1G>T
ENST00000648635.1:c.*327+1G>T	ENSP00000497204.1:n.*327+1G>T
ENST00000648743.1:c.343+1G>T	ENSP00000497135.1:n.343+1G>T
ENST00000649011.1:c.628+1G>T	ENSP00000497575.1:n.628+1G>T
ENST00000649028.1:c.343+1G>T	ENSP00000498034.1:n.343+1G>T
ENST00000649054.1:c.343+1G>T	ENSP00000496991.1:n.343+1G>T
ENST00000649057.1:c.*127+1G>T	ENSP00000497639.1:n.*127+1G>T
ENST00000649166.1:c.*246+1G>T	ENSP00000496844.1:n.*246+1G>T
ENST00000649370.1:n.371+1G>T
ENST00000649673.1:c.562+1G>T	ENSP00000497864.1:n.562+1G>T
ENST00000649679.1:c.343+1G>T	ENSP00000497387.1:n.343+1G>T
ENST00000649744.1:n.750+1G>T
ENST00000649795.1:c.*149+1G>T	ENSP00000498147.1:n.*149+1G>T
ENST00000649918.1:c.343+1G>T	ENSP00000497487.1:n.343+1G>T
ENST00000649958.1:c.*72+1G>T	ENSP00000496827.1:n.*72+1G>T
ENST00000649970.1:c.366+1G>T
ENST00000650035.1:c.343+1G>T	ENSP00000497703.1:n.343+1G>T
ENST00000650043.1:n.541+1G>T
ENST00000650107.1:c.343+1G>T	ENSP00000497124.1:n.343+1G>T
ENST00000650124.1:c.*72+1G>T	ENSP00000497903.1:n.*72+1G>T
ENST00000650473.1:c.315+1G>T	ENSP00000497045.1:n.315+1G>T
XM_006715511.2:c.-51+1G>T	XP_006715574.1:n.-51+1G>T
XM_011535941.1:c.343+1G>T	XP_011534243.1:n.343+1G>T
XM_024446488.1:c.343+1G>T	XP_024302256.1:n.343+1G>T