Canonical Allele Identifier: CA15090654

Gene: LBR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.225412341C>T , CM000663.2:g.225412341C>T	GRCh38
NC_000001.10:g.225600043C>T , CM000663.1:g.225600043C>T	GRCh37
NC_000001.9:g.223666666C>T	NCBI36
NG_008099.1:g.21477G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002296.4:c.1084+113G>A MANE Select	NP_002287.2:n.1084+113G>A
ENST00000272163.9:c.1084+113G>A MANE Select	ENSP00000272163.4:n.1084+113G>A
NM_002296.3:c.1084+113G>A	NP_002287.2:n.1084+113G>A
NM_194442.2:c.1084+113G>A	NP_919424.1:n.1084+113G>A
NM_194442.3:c.1084+113G>A	NP_919424.1:n.1084+113G>A
ENST00000272163.8:c.1084+113G>A	ENSP00000272163.4:n.1084+113G>A
ENST00000338179.6:c.1084+113G>A	ENSP00000339883.2:n.1084+113G>A
ENST00000651341.1:c.1084+113G>A	ENSP00000499114.1:n.1084+113G>A
XM_005273125.2:c.1084+113G>A	XP_005273182.1:n.1084+113G>A
XM_005273125.3:c.1084+113G>A	XP_005273182.1:n.1084+113G>A
XM_011544185.1:c.1084+113G>A	XP_011542487.1:n.1084+113G>A
XM_011544185.3:c.1084+113G>A	XP_011542487.1:n.1084+113G>A
XM_011544186.1:c.1084+113G>A	XP_011542488.1:n.1084+113G>A
XM_011544187.1:c.1084+113G>A	XP_011542489.1:n.1084+113G>A
XR_001737168.2:n.1211+113G>A