Canonical Allele Identifier: CA256190530
Gene: LIG4 HGNC NCBI

Linked Data

dbSNP Id: rs774932573

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108214606_108214613del , CM000675.2:g.108214606_108214613del GRCh38
NC_000013.10:g.108866954_108866961del , CM000675.1:g.108866954_108866961del GRCh37
NC_000013.9:g.107664955_107664962del NCBI36
NG_007396.1:g.5924_5931del , LRG_79:g.5924_5931del

Transcript Alleles

HGVS Amino-acid Change
ENST00000614526.2:c.-222-1_-216del
ENST00000685338.1:c.-78_-71del ENSP00000510567.1:n.-78_-71del
ENST00000686095.1:c.-102_-95del ENSP00000509942.1:n.-102_-95del
ENST00000686204.1:c.-78_-71del ENSP00000509685.1:n.-78_-71del
ENST00000686913.1:c.-102_-95del ENSP00000509299.1:n.-102_-95del
ENST00000686926.1:c.-29+873_-29+880del ENSP00000509122.1:n.-29+873_-29+880del
ENST00000687164.1:c.-101-1_-95del
ENST00000687822.1:c.-102_-95del ENSP00000509344.1:n.-102_-95del
ENST00000688396.1:c.-102_-95del ENSP00000509564.1:n.-102_-95del
ENST00000688455.1:c.-101-1_-95del
ENST00000688529.1:c.-102_-95del ENSP00000509906.1:n.-102_-95del
ENST00000688595.1:c.-78_-71del ENSP00000509502.1:n.-78_-71del
ENST00000689762.1:c.-223_-216del ENSP00000508867.1:n.-223_-216del
ENST00000690127.1:c.-223_-216del ENSP00000509468.1:n.-223_-216del
ENST00000692222.1:c.-101-1_-95del
ENST00000693040.1:c.-77-1_-71del
ENST00000442234.6:c.-101-1_-95del
ENST00000356922.5:c.-102_-95del ENSP00000349393.3:n.-102_-95del
ENST00000405925.2:c.-28-3315_-28-3308del ENSP00000385955.1:n.-28-3315_-28-3308del
ENST00000442234.5:c.-101-1_-95del
ENST00000611712.4:c.-102_-95del ENSP00000484288.1:n.-102_-95del
ENST00000614526.1:c.-222-1_-216del
NM_001098268.1:c.-28-3315_-28-3308del NP_001091738.1:n.-28-3315_-28-3308del
NM_002312.3:c.-102_-95del , LRG_79t1:c.-102_-95del NP_002303.2:n.-102_-95del
NM_206937.1:c.-101-1_-95del
XM_005254056.1:c.-77-1_-71del
XM_005254057.3:c.-102_-95del XP_005254114.1:n.-102_-95del
XM_005254058.2:c.-29+873_-29+880del XP_005254115.1:n.-29+873_-29+880del
XM_006719951.2:c.-102_-95del XP_006720014.1:n.-102_-95del
XM_006719952.1:c.-78_-71del XP_006720015.1:n.-78_-71del
XM_011521091.1:c.-102_-95del XP_011519393.1:n.-102_-95del
XM_011521092.1:c.-101-1_-95del
NM_001330595.1:c.-222-1_-216del
NM_001352598.1:c.-78_-71del NP_001339527.1:n.-78_-71del
NM_001352599.1:c.-102_-95del NP_001339528.1:n.-102_-95del
NM_001352600.1:c.-101-1_-95del
NM_001352601.1:c.-102_-95del NP_001339530.1:n.-102_-95del
NM_001352602.1:c.-101-1_-95del
NM_001352603.1:c.-101-1_-95del
NM_001352604.1:c.15_22del NP_001339533.1:p.Gln5HisfsTer16
XM_005254058.4:c.-29+873_-29+880del XP_005254115.1:n.-29+873_-29+880del
XM_006719951.3:c.-102_-95del XP_006720014.1:n.-102_-95del
XM_017020564.1:c.15_22del XP_016876053.1:p.Gln5HisfsTer16
XM_017020565.1:c.15_22del XP_016876054.1:p.Gln5HisfsTer16
XM_017020566.1:c.15_22del XP_016876055.1:p.Gln5HisfsTer16
XM_017020568.2:c.15_22del XP_016876057.1:p.Gln5HisfsTer27
XM_017020571.1:c.-78_-71del XP_016876060.1:n.-78_-71del
XM_017020573.1:c.-222-1_-216del
NM_001098268.2:c.-28-3315_-28-3308del NP_001091738.1:n.-28-3315_-28-3308del
NM_001352598.2:c.-78_-71del NP_001339527.1:n.-78_-71del
NM_001352599.2:c.-102_-95del NP_001339528.1:n.-102_-95del
NM_001352600.2:c.-101-1_-95del
NM_001352601.2:c.-102_-95del NP_001339530.1:n.-102_-95del
NM_001352602.2:c.-101-1_-95del
NM_206937.2:c.-101-1_-95del
NM_001330595.2:c.-222-1_-216del
NM_001352604.2:c.15_22del NP_001339533.1:p.Gln5HisfsTer16
NM_001379095.1:c.-102_-95del NP_001366024.1:n.-102_-95del