Canonical Allele Identifier: CA388624833

Gene: LIG4

Linked Data

• ClinVar Variation Id: 1338155
• ClinVar RCV Id: RCV001822753
• dbSNP Id: rs1805388
• MyVariant Identifiers: chr13:g.108863591G>C (hg19) ; chr13:g.108211243G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.108211243G>C , CM000675.2:g.108211243G>C	GRCh38
NC_000013.10:g.108863591G>C , CM000675.1:g.108863591G>C	GRCh37
NC_000013.9:g.107661592G>C	NCBI36
NG_007396.1:g.9292C>G , LRG_79:g.9292C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614526.2:c.-149-27C>G	ENSP00000480814.1:n.-149-27C>G
ENST00000685338.1:c.26C>G	ENSP00000510567.1:p.Thr9Ser
ENST00000686095.1:c.26C>G	ENSP00000509942.1:p.Thr9Ser
ENST00000686204.1:c.26C>G	ENSP00000509685.1:p.Thr9Ser
ENST00000686913.1:c.26C>G	ENSP00000509299.1:p.Thr9Ser
ENST00000686926.1:c.26C>G	ENSP00000509122.1:p.Thr9Ser
ENST00000687164.1:c.26C>G	ENSP00000508512.1:p.Thr9Ser
ENST00000687822.1:c.26C>G	ENSP00000509344.1:p.Thr9Ser
ENST00000688396.1:c.26C>G	ENSP00000509564.1:p.Thr9Ser
ENST00000688455.1:c.26C>G	ENSP00000509304.1:p.Thr9Ser
ENST00000688529.1:c.26C>G	ENSP00000509906.1:p.Thr9Ser
ENST00000688595.1:c.26C>G	ENSP00000509502.1:p.Thr9Ser
ENST00000689762.1:c.-149-27C>G	ENSP00000508867.1:n.-149-27C>G
ENST00000690127.1:c.-149-27C>G	ENSP00000509468.1:n.-149-27C>G
ENST00000692222.1:c.26C>G	ENSP00000509226.1:p.Thr9Ser
ENST00000693040.1:c.26C>G	ENSP00000510014.1:p.Thr9Ser
ENST00000442234.6:c.26C>G MANE Select	ENSP00000402030.1:p.Thr9Ser
ENST00000356922.5:c.26C>G	ENSP00000349393.3:p.Thr9Ser
ENST00000405925.2:c.26C>G	ENSP00000385955.1:p.Thr9Ser
ENST00000442234.5:c.26C>G	ENSP00000402030.1:p.Thr9Ser
ENST00000611712.4:c.26C>G	ENSP00000484288.1:p.Thr9Ser
ENST00000614526.1:c.-149-27C>G	ENSP00000480814.1:n.-149-27C>G
NM_001098268.1:c.26C>G	NP_001091738.1:p.Thr9Ser
NM_002312.3:c.26C>G , LRG_79t1:c.26C>G	NP_002303.2:p.Thr9Ser
NM_206937.1:c.26C>G	NP_996820.1:p.Thr9Ser
XM_005254056.1:c.26C>G	XP_005254113.1:p.Thr9Ser
XM_005254057.3:c.26C>G	XP_005254114.1:p.Thr9Ser
XM_005254058.2:c.26C>G	XP_005254115.1:p.Thr9Ser
XM_006719951.2:c.26C>G	XP_006720014.1:p.Thr9Ser
XM_006719952.1:c.26C>G	XP_006720015.1:p.Thr9Ser
XM_011521091.1:c.26C>G	XP_011519393.1:p.Thr9Ser
XM_011521092.1:c.26C>G	XP_011519394.1:p.Thr9Ser
NM_001330595.1:c.-149-27C>G	NP_001317524.1:n.-149-27C>G
NM_001352598.1:c.26C>G	NP_001339527.1:p.Thr9Ser
NM_001352599.1:c.26C>G	NP_001339528.1:p.Thr9Ser
NM_001352600.1:c.26C>G	NP_001339529.1:p.Thr9Ser
NM_001352601.1:c.26C>G	NP_001339530.1:p.Thr9Ser
NM_001352602.1:c.26C>G	NP_001339531.1:p.Thr9Ser
NM_001352603.1:c.26C>G	NP_001339532.1:p.Thr9Ser
NM_001352604.1:c.89-27C>G	NP_001339533.1:n.89-27C>G
XM_005254058.4:c.26C>G	XP_005254115.1:p.Thr9Ser
XM_006719951.3:c.26C>G	XP_006720014.1:p.Thr9Ser
XM_017020564.1:c.89-27C>G	XP_016876053.1:n.89-27C>G
XM_017020565.1:c.89-27C>G	XP_016876054.1:n.89-27C>G
XM_017020566.1:c.89-27C>G	XP_016876055.1:n.89-27C>G
XM_017020568.2:c.65-27C>G	XP_016876057.1:n.65-27C>G
XM_017020571.1:c.26C>G	XP_016876060.1:p.Thr9Ser
XM_017020573.1:c.-149-27C>G	XP_016876062.1:n.-149-27C>G
NM_001098268.2:c.26C>G	NP_001091738.1:p.Thr9Ser
NM_001352598.2:c.26C>G	NP_001339527.1:p.Thr9Ser
NM_001352599.2:c.26C>G	NP_001339528.1:p.Thr9Ser
NM_001352600.2:c.26C>G	NP_001339529.1:p.Thr9Ser
NM_001352601.2:c.26C>G	NP_001339530.1:p.Thr9Ser
NM_001352602.2:c.26C>G	NP_001339531.1:p.Thr9Ser
NM_206937.2:c.26C>G MANE Select	NP_996820.1:p.Thr9Ser
NM_001330595.2:c.-149-27C>G	NP_001317524.1:n.-149-27C>G
NM_001352604.2:c.89-27C>G	NP_001339533.1:n.89-27C>G
NM_001379095.1:c.26C>G	NP_001366024.1:p.Thr9Ser