Canonical Allele Identifier: CA2257315285
Community Standard Title: NM_013975.4(LIG3):c.*50C=
Gene: LIG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35004556C= , CM000679.2:g.35004556C= GRCh38
NC_000017.10:g.33331575C= , CM000679.1:g.33331575C= GRCh37
NC_000017.9:g.30355688C= NCBI36
NG_029221.1:g.29059C=

Transcript Alleles

HGVS Amino-acid Change
NM_013975.4:c.*50C= MANE Select NP_039269.2:n.*50C=
ENST00000378526.9:c.*50C= MANE Select ENSP00000367787.3:n.*50C=
NM_013975.3:c.*50C= NP_039269.2:n.*50C=
ENST00000378526.8:c.*50C= ENSP00000367787.3:n.*50C=
ENST00000593099.5:n.4416C=
XM_005257970.2:c.*50C= XP_005258027.1:n.*50C=
XM_005257970.4:c.*50C= XP_005258027.1:n.*50C=
XM_011524797.1:c.2823+1767C= XP_011523099.1:n.2823+1767C=
XM_011524798.1:c.2796+1767C= XP_011523100.1:n.2796+1767C=
XM_011524799.1:c.2796+1767C= XP_011523101.1:n.2796+1767C=
XM_011524800.1:c.2823+1767C= XP_011523102.1:n.2823+1767C=
XM_017024624.1:c.*50C= XP_016880113.1:n.*50C=