Canonical Allele Identifier: CA2257312223

Gene: LIG3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35002629G= , CM000679.2:g.35002629G=	GRCh38
NC_000017.10:g.33329648G= , CM000679.1:g.33329648G=	GRCh37
NC_000017.9:g.30353761G=	NCBI36
NG_029221.1:g.27132G=

Transcript Alleles

HGVS	Amino-acid Change
NM_013975.4:c.2675-39G= MANE Select	NP_039269.2:n.2675-39G=
ENST00000378526.9:c.2675-39G= MANE Select	ENSP00000367787.3:n.2675-39G=
NM_002311.4:c.2675-39G=	NP_002302.2:n.2675-39G=
NM_002311.5:c.2675-39G=	NP_002302.2:n.2675-39G=
NM_013975.3:c.2675-39G=	NP_039269.2:n.2675-39G=
ENST00000262327.9:c.2675-39G=	ENSP00000262327.4:n.2675-39G=
ENST00000378526.8:c.2675-39G=	ENSP00000367787.3:n.2675-39G=
ENST00000593099.5:n.2528-39G=
XM_005257970.2:c.2702-39G=	XP_005258027.1:n.2702-39G=
XM_005257970.4:c.2702-39G=	XP_005258027.1:n.2702-39G=
XM_006721896.2:c.2702-39G=	XP_006721959.1:n.2702-39G=
XM_006721896.3:c.2702-39G=	XP_006721959.1:n.2702-39G=
XM_011524797.1:c.2702-39G=	XP_011523099.1:n.2702-39G=
XM_011524798.1:c.2675-39G=	XP_011523100.1:n.2675-39G=
XM_011524799.1:c.2675-39G=	XP_011523101.1:n.2675-39G=
XM_011524800.1:c.2702-39G=	XP_011523102.1:n.2702-39G=
XM_017024624.1:c.2675-39G=	XP_016880113.1:n.2675-39G=