Canonical Allele Identifier: CA1224457311

Gene: LBR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.225403404G= , CM000663.2:g.225403404G=	GRCh38
NC_000001.10:g.225591106G= , CM000663.1:g.225591106G=	GRCh37
NC_000001.9:g.223657729G=	NCBI36
NG_008099.1:g.30414C=

Transcript Alleles

HGVS	Amino-acid Change
NM_002296.4:c.1747C= MANE Select	NP_002287.2:p.Arg583=
ENST00000272163.9:c.1747C= MANE Select	ENSP00000272163.4:p.Arg583=
NM_002296.3:c.1747C=	NP_002287.2:p.Arg583=
NM_194442.2:c.1747C=	NP_919424.1:p.Arg583=
NM_194442.3:c.1747C=	NP_919424.1:p.Arg583=
ENST00000272163.8:c.1747C=	ENSP00000272163.4:p.Arg583=
ENST00000338179.6:c.1747C=	ENSP00000339883.2:p.Arg583=
ENST00000441022.1:n.222C=
ENST00000651341.1:c.*913C=	ENSP00000499114.1:n.*913C=
XM_005273125.2:c.1621C=	XP_005273182.1:p.Arg541=
XM_005273125.3:c.1621C=	XP_005273182.1:p.Arg541=
XM_011544185.1:c.1747C=	XP_011542487.1:p.Arg583=
XM_011544185.3:c.1747C=	XP_011542487.1:p.Arg583=
XM_011544186.1:c.1666C=	XP_011542488.1:p.Arg556=
XR_001737168.2:n.1770C=