Canonical Allele Identifier: CA2117796423
Gene: LIG4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108214557G= , CM000675.2:g.108214557G= GRCh38
NC_000013.10:g.108866905G= , CM000675.1:g.108866905G= GRCh37
NC_000013.9:g.107664906G= NCBI36
NG_007396.1:g.5978C= , LRG_79:g.5978C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000614526.2:c.-169C= ENSP00000480814.1:n.-169C=
ENST00000685338.1:c.-29+5C= ENSP00000510567.1:n.-29+5C=
ENST00000686095.1:c.-48C= ENSP00000509942.1:n.-48C=
ENST00000686204.1:c.-29+5C= ENSP00000509685.1:n.-29+5C=
ENST00000686913.1:c.-48C= ENSP00000509299.1:n.-48C=
ENST00000686926.1:c.-29+927C= ENSP00000509122.1:n.-29+927C=
ENST00000687164.1:c.-48C= ENSP00000508512.1:n.-48C=
ENST00000687822.1:c.-48C= ENSP00000509344.1:n.-48C=
ENST00000688396.1:c.-48C= ENSP00000509564.1:n.-48C=
ENST00000688455.1:c.-48C= ENSP00000509304.1:n.-48C=
ENST00000688529.1:c.-48C= ENSP00000509906.1:n.-48C=
ENST00000688595.1:c.-29+5C= ENSP00000509502.1:n.-29+5C=
ENST00000689762.1:c.-169C= ENSP00000508867.1:n.-169C=
ENST00000690127.1:c.-169C= ENSP00000509468.1:n.-169C=
ENST00000692222.1:c.-48C= ENSP00000509226.1:n.-48C=
ENST00000693040.1:c.-29+5C= ENSP00000510014.1:n.-29+5C=
ENST00000442234.6:c.-48C= MANE Select ENSP00000402030.1:n.-48C=
ENST00000356922.5:c.-48C= ENSP00000349393.3:n.-48C=
ENST00000405925.2:c.-28-3261C= ENSP00000385955.1:n.-28-3261C=
ENST00000442234.5:c.-48C= ENSP00000402030.1:n.-48C=
ENST00000611712.4:c.-48C= ENSP00000484288.1:n.-48C=
ENST00000614526.1:c.-169C= ENSP00000480814.1:n.-169C=
NM_001098268.1:c.-28-3261C= NP_001091738.1:n.-28-3261C=
NM_002312.3:c.-48C= , LRG_79t1:c.-48C= NP_002303.2:n.-48C=
NM_206937.1:c.-48C= NP_996820.1:n.-48C=
XM_005254056.1:c.-29+5C= XP_005254113.1:n.-29+5C=
XM_005254057.3:c.-48C= XP_005254114.1:n.-48C=
XM_005254058.2:c.-29+927C= XP_005254115.1:n.-29+927C=
XM_006719951.2:c.-48C= XP_006720014.1:n.-48C=
XM_006719952.1:c.-29+5C= XP_006720015.1:n.-29+5C=
XM_011521091.1:c.-48C= XP_011519393.1:n.-48C=
XM_011521092.1:c.-48C= XP_011519394.1:n.-48C=
NM_001330595.1:c.-169C= NP_001317524.1:n.-169C=
NM_001352598.1:c.-29+5C= NP_001339527.1:n.-29+5C=
NM_001352599.1:c.-48C= NP_001339528.1:n.-48C=
NM_001352600.1:c.-48C= NP_001339529.1:n.-48C=
NM_001352601.1:c.-48C= NP_001339530.1:n.-48C=
NM_001352602.1:c.-48C= NP_001339531.1:n.-48C=
NM_001352603.1:c.-48C= NP_001339532.1:n.-48C=
NM_001352604.1:c.69C= NP_001339533.1:p.Asn23=
XM_005254058.4:c.-29+927C= XP_005254115.1:n.-29+927C=
XM_006719951.3:c.-48C= XP_006720014.1:n.-48C=
XM_017020564.1:c.69C= XP_016876053.1:p.Asn23=
XM_017020565.1:c.69C= XP_016876054.1:p.Asn23=
XM_017020566.1:c.69C= XP_016876055.1:p.Asn23=
XM_017020568.2:c.64+5C= XP_016876057.1:n.64+5C=
XM_017020571.1:c.-29+5C= XP_016876060.1:n.-29+5C=
XM_017020573.1:c.-169C= XP_016876062.1:n.-169C=
NM_001098268.2:c.-28-3261C= NP_001091738.1:n.-28-3261C=
NM_001352598.2:c.-29+5C= NP_001339527.1:n.-29+5C=
NM_001352599.2:c.-48C= NP_001339528.1:n.-48C=
NM_001352600.2:c.-48C= NP_001339529.1:n.-48C=
NM_001352601.2:c.-48C= NP_001339530.1:n.-48C=
NM_001352602.2:c.-48C= NP_001339531.1:n.-48C=
NM_206937.2:c.-48C= MANE Select NP_996820.1:n.-48C=
NM_001330595.2:c.-169C= NP_001317524.1:n.-169C=
NM_001352604.2:c.69C= NP_001339533.1:p.Asn23=
NM_001379095.1:c.-48C= NP_001366024.1:n.-48C=