Canonical Allele Identifier: CA15905891

Gene: LIG3

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.34988426G>A , CM000679.2:g.34988426G>A	GRCh38
NC_000017.10:g.33315445G>A , CM000679.1:g.33315445G>A	GRCh37
NC_000017.9:g.30339558G>A	NCBI36
NG_029221.1:g.12929G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378526.9:c.692-1040G>A MANE Select	ENSP00000367787.3:n.692-1040G>A
ENST00000262327.9:c.692-1040G>A	ENSP00000262327.4:n.692-1040G>A
ENST00000378526.8:c.692-1040G>A	ENSP00000367787.3:n.692-1040G>A
ENST00000585740.5:c.-122-1040G>A	ENSP00000467757.1:n.-122-1040G>A
ENST00000585941.5:c.719-1040G>A	ENSP00000468479.1:n.719-1040G>A
ENST00000586407.1:n.741-1040G>A
ENST00000586435.1:n.39-1040G>A
ENST00000588109.5:c.292-1040G>A
ENST00000590181.5:n.742-1040G>A
ENST00000592690.1:c.431-1040G>A	ENSP00000467063.1:n.431-1040G>A
NM_002311.4:c.692-1040G>A	NP_002302.2:n.692-1040G>A
NM_013975.3:c.692-1040G>A	NP_039269.2:n.692-1040G>A
XM_005257970.2:c.719-1040G>A	XP_005258027.1:n.719-1040G>A
XM_006721896.2:c.719-1040G>A	XP_006721959.1:n.719-1040G>A
XM_011524797.1:c.719-1040G>A	XP_011523099.1:n.719-1040G>A
XM_011524798.1:c.692-1040G>A	XP_011523100.1:n.692-1040G>A
XM_011524799.1:c.692-1040G>A	XP_011523101.1:n.692-1040G>A
XM_011524800.1:c.719-1040G>A	XP_011523102.1:n.719-1040G>A
XM_005257970.4:c.719-1040G>A	XP_005258027.1:n.719-1040G>A
XM_006721896.3:c.719-1040G>A	XP_006721959.1:n.719-1040G>A
XM_017024624.1:c.692-1040G>A	XP_016880113.1:n.692-1040G>A
NM_013975.4:c.692-1040G>A MANE Select	NP_039269.2:n.692-1040G>A
NM_002311.5:c.692-1040G>A	NP_002302.2:n.692-1040G>A