Canonical Allele Identifier: CA3880062

Gene: LMBRD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.69796899A>T , CM000668.2:g.69796899A>T	GRCh38
NC_000006.11:g.70506791A>T , CM000668.1:g.70506791A>T	GRCh37
NC_000006.10:g.70563512A>T	NCBI36
NG_016012.1:g.5259T>A
NG_016012.2:g.74718T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_018368.4:c.-18T>A MANE Select	NP_060838.3:n.-18T>A
ENST00000649934.3:c.-18T>A MANE Select	ENSP00000497690.1:n.-18T>A
NM_018368.3:c.-18T>A	NP_060838.3:n.-18T>A
ENST00000370577.7:c.-18T>A	ENSP00000359609.3:n.-18T>A
ENST00000647650.1:c.-18T>A	ENSP00000497808.1:n.-18T>A
ENST00000647934.1:n.390-6427T>A
ENST00000647964.1:c.-150-6427T>A	ENSP00000496784.1:n.-150-6427T>A
ENST00000648303.1:c.-18T>A	ENSP00000498133.1:n.-18T>A
ENST00000648330.1:n.352T>A
ENST00000648394.1:c.-150-6427T>A	ENSP00000497302.1:n.-150-6427T>A
ENST00000649011.1:c.-18T>A	ENSP00000497575.1:n.-18T>A
ENST00000649028.1:c.-150-6427T>A	ENSP00000498034.1:n.-150-6427T>A
ENST00000649744.1:n.258-6427T>A
ENST00000649795.1:c.-18T>A	ENSP00000498147.1:n.-18T>A
ENST00000649918.1:c.-150-6427T>A	ENSP00000497487.1:n.-150-6427T>A
ENST00000649958.1:c.-18T>A	ENSP00000496827.1:n.-18T>A
ENST00000650035.1:c.-151+1216T>A	ENSP00000497703.1:n.-151+1216T>A
ENST00000650107.1:c.-150-6427T>A	ENSP00000497124.1:n.-150-6427T>A