Canonical Allele Identifier: CA1417354
Gene: LBR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.225415348dup , CM000663.2:g.225415348dup GRCh38
NC_000001.10:g.225603050dup , CM000663.1:g.225603050dup GRCh37
NC_000001.9:g.223669673dup NCBI36
NG_008099.1:g.18477dup

Transcript Alleles

HGVS Amino-acid Change
NM_002296.4:c.838-9dup MANE Select NP_002287.2:n.838-9dup
ENST00000272163.9:c.838-9dup MANE Select ENSP00000272163.4:n.838-9dup
NM_002296.3:c.838-9dup NP_002287.2:n.838-9dup
NM_194442.2:c.838-9dup NP_919424.1:n.838-9dup
NM_194442.3:c.838-9dup NP_919424.1:n.838-9dup
ENST00000272163.8:c.838-9dup ENSP00000272163.4:n.838-9dup
ENST00000338179.6:c.838-9dup ENSP00000339883.2:n.838-9dup
ENST00000651341.1:c.838-9dup ENSP00000499114.1:n.838-9dup
XM_005273125.2:c.838-9dup XP_005273182.1:n.838-9dup
XM_005273125.3:c.838-9dup XP_005273182.1:n.838-9dup
XM_011544185.1:c.838-9dup XP_011542487.1:n.838-9dup
XM_011544185.3:c.838-9dup XP_011542487.1:n.838-9dup
XM_011544186.1:c.838-9dup XP_011542488.1:n.838-9dup
XM_011544187.1:c.838-9dup XP_011542489.1:n.838-9dup
XR_001737168.2:n.965-9dup