Canonical Allele Identifier: CA1417287

Gene: LBR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.225412611G>A , CM000663.2:g.225412611G>A	GRCh38
NC_000001.10:g.225600313G>A , CM000663.1:g.225600313G>A	GRCh37
NC_000001.9:g.223666936G>A	NCBI36
NG_008099.1:g.21207C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272163.9:c.927C>T MANE Select	ENSP00000272163.4:p.Ile309=
ENST00000651341.1:c.927C>T	ENSP00000499114.1:p.Ile309=
ENST00000272163.8:c.927C>T	ENSP00000272163.4:p.Ile309=
ENST00000338179.6:c.927C>T	ENSP00000339883.2:p.Ile309=
NM_002296.3:c.927C>T	NP_002287.2:p.Ile309=
NM_194442.2:c.927C>T	NP_919424.1:p.Ile309=
XM_005273125.2:c.927C>T	XP_005273182.1:p.Ile309=
XM_011544185.1:c.927C>T	XP_011542487.1:p.Ile309=
XM_011544186.1:c.927C>T	XP_011542488.1:p.Ile309=
XM_011544187.1:c.927C>T	XP_011542489.1:p.Ile309=
XM_005273125.3:c.927C>T	XP_005273182.1:p.Ile309=
XM_011544185.3:c.927C>T	XP_011542487.1:p.Ile309=
XR_001737168.2:n.1054C>T
NM_002296.4:c.927C>T MANE Select	NP_002287.2:p.Ile309=
NM_194442.3:c.927C>T	NP_919424.1:p.Ile309=