Canonical Allele Identifier: CA3880050

Gene: LMBRD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.69796861G>A , CM000668.2:g.69796861G>A	GRCh38
NC_000006.11:g.70506753G>A , CM000668.1:g.70506753G>A	GRCh37
NC_000006.10:g.70563474G>A	NCBI36
NG_016012.1:g.5297C>T
NG_016012.2:g.74756C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_018368.4:c.21C>T MANE Select	NP_060838.3:p.Ala7=
ENST00000649934.3:c.21C>T MANE Select	ENSP00000497690.1:p.Ala7=
NM_018368.3:c.21C>T	NP_060838.3:p.Ala7=
ENST00000370577.7:c.21C>T	ENSP00000359609.3:p.Ala7=
ENST00000472827.1:c.21C>T	ENSP00000433385.1:p.Ala7=
ENST00000472827.2:c.21C>T	ENSP00000433385.2:p.Ala7=
ENST00000647650.1:c.21C>T	ENSP00000497808.1:p.Ala7=
ENST00000647934.1:n.390-6389C>T
ENST00000647964.1:c.-150-6389C>T	ENSP00000496784.1:n.-150-6389C>T
ENST00000648303.1:c.21C>T	ENSP00000498133.1:p.Ala7=
ENST00000648330.1:n.390C>T
ENST00000648394.1:c.-150-6389C>T	ENSP00000497302.1:n.-150-6389C>T
ENST00000649011.1:c.21C>T	ENSP00000497575.1:p.Ala7=
ENST00000649028.1:c.-150-6389C>T	ENSP00000498034.1:n.-150-6389C>T
ENST00000649166.1:c.21C>T	ENSP00000496844.1:p.Ala7=
ENST00000649673.1:c.21C>T	ENSP00000497864.1:p.Ala7=
ENST00000649744.1:n.258-6389C>T
ENST00000649795.1:c.21C>T	ENSP00000498147.1:p.Ala7=
ENST00000649918.1:c.-150-6389C>T	ENSP00000497487.1:n.-150-6389C>T
ENST00000649958.1:c.21C>T	ENSP00000496827.1:p.Ala7=
ENST00000650035.1:c.-151+1254C>T	ENSP00000497703.1:n.-151+1254C>T
ENST00000650107.1:c.-150-6389C>T	ENSP00000497124.1:n.-150-6389C>T
ENST00000650124.1:c.21C>T	ENSP00000497903.1:p.Ala7=