Canonical Allele Identifier: CA1417522

Gene: LBR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.225422181C>T , CM000663.2:g.225422181C>T	GRCh38
NC_000001.10:g.225609883C>T , CM000663.1:g.225609883C>T	GRCh37
NC_000001.9:g.223676506C>T	NCBI36
NG_008099.1:g.11637G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272163.9:c.262G>A MANE Select	ENSP00000272163.4:p.Gly88Ser
ENST00000651341.1:c.262G>A	ENSP00000499114.1:p.Gly88Ser
ENST00000272163.8:c.262G>A	ENSP00000272163.4:p.Gly88Ser
ENST00000338179.6:c.262G>A	ENSP00000339883.2:p.Gly88Ser
ENST00000425080.1:c.262G>A	ENSP00000388059.1:p.Gly88Ser
ENST00000488632.1:n.247G>A
NM_002296.3:c.262G>A	NP_002287.2:p.Gly88Ser
NM_194442.2:c.262G>A	NP_919424.1:p.Gly88Ser
XM_005273125.2:c.262G>A	XP_005273182.1:p.Gly88Ser
XM_011544185.1:c.262G>A	XP_011542487.1:p.Gly88Ser
XM_011544186.1:c.262G>A	XP_011542488.1:p.Gly88Ser
XM_011544187.1:c.262G>A	XP_011542489.1:p.Gly88Ser
XM_005273125.3:c.262G>A	XP_005273182.1:p.Gly88Ser
XM_011544185.3:c.262G>A	XP_011542487.1:p.Gly88Ser
XR_001737168.2:n.389G>A
NM_002296.4:c.262G>A MANE Select	NP_002287.2:p.Gly88Ser
NM_194442.3:c.262G>A	NP_919424.1:p.Gly88Ser