Canonical Allele Identifier: CA1417296
Gene: LBR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.225412665del , CM000663.2:g.225412665del GRCh38
NC_000001.10:g.225600367del , CM000663.1:g.225600367del GRCh37
NC_000001.9:g.223666990del NCBI36
NG_008099.1:g.21168del

Transcript Alleles

HGVS Amino-acid Change
ENST00000272163.9:c.893-5del MANE Select ENSP00000272163.4:n.893-5del
ENST00000651341.1:c.893-5del ENSP00000499114.1:n.893-5del
ENST00000272163.8:c.893-5del ENSP00000272163.4:n.893-5del
ENST00000338179.6:c.893-5del ENSP00000339883.2:n.893-5del
NM_002296.3:c.893-5del NP_002287.2:n.893-5del
NM_194442.2:c.893-5del NP_919424.1:n.893-5del
XM_005273125.2:c.893-5del XP_005273182.1:n.893-5del
XM_011544185.1:c.893-5del XP_011542487.1:n.893-5del
XM_011544186.1:c.893-5del XP_011542488.1:n.893-5del
XM_011544187.1:c.893-5del XP_011542489.1:n.893-5del
XM_005273125.3:c.893-5del XP_005273182.1:n.893-5del
XM_011544185.3:c.893-5del XP_011542487.1:n.893-5del
XR_001737168.2:n.1020-5del
NM_002296.4:c.893-5del MANE Select NP_002287.2:n.893-5del
NM_194442.3:c.893-5del NP_919424.1:n.893-5del