Canonical Allele Identifier: CA256190989

Gene: LIG4

Linked Data

• dbSNP Id: rs3093739
• gnomAD v2: 13-108867401-A-G
• gnomAD v3: 13-108215053-A-G
• gnomAD v4: 13-108215053-A-G
• MyVariant Identifiers: chr13:g.108867401A>G (hg19) ; chr13:g.108215053A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.108215053A>G , CM000675.2:g.108215053A>G	GRCh38
NC_000013.10:g.108867401A>G , CM000675.1:g.108867401A>G	GRCh37
NC_000013.9:g.107665402A>G	NCBI36
NG_007396.1:g.5482T>C , LRG_79:g.5482T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000614526.2:c.-223+431T>C	ENSP00000480814.1:n.-223+431T>C
ENST00000685338.1:c.-274-246T>C	ENSP00000510567.1:n.-274-246T>C
ENST00000686095.1:c.-210+107T>C	ENSP00000509942.1:n.-210+107T>C
ENST00000686204.1:c.-185-335T>C	ENSP00000509685.1:n.-185-335T>C
ENST00000686913.1:c.-298-246T>C	ENSP00000509299.1:n.-298-246T>C
ENST00000686926.1:c.-29+431T>C	ENSP00000509122.1:n.-29+431T>C
ENST00000687164.1:c.-102+271T>C	ENSP00000508512.1:n.-102+271T>C
ENST00000687822.1:c.-209-335T>C	ENSP00000509344.1:n.-209-335T>C
ENST00000688396.1:c.-209-335T>C	ENSP00000509564.1:n.-209-335T>C
ENST00000688455.1:c.-102+431T>C	ENSP00000509304.1:n.-102+431T>C
ENST00000688529.1:c.-210+271T>C	ENSP00000509906.1:n.-210+271T>C
ENST00000688595.1:c.-185-335T>C	ENSP00000509502.1:n.-185-335T>C
ENST00000689762.1:c.-330-335T>C	ENSP00000508867.1:n.-330-335T>C
ENST00000690127.1:c.-331+271T>C	ENSP00000509468.1:n.-331+271T>C
ENST00000692222.1:c.-102+431T>C	ENSP00000509226.1:n.-102+431T>C
ENST00000693040.1:c.-78+431T>C	ENSP00000510014.1:n.-78+431T>C
ENST00000442234.6:c.-102+431T>C MANE Select	ENSP00000402030.1:n.-102+431T>C
ENST00000405925.2:c.-29+3109T>C	ENSP00000385955.1:n.-29+3109T>C
ENST00000442234.5:c.-102+431T>C	ENSP00000402030.1:n.-102+431T>C
ENST00000611712.4:c.-298-246T>C	ENSP00000484288.1:n.-298-246T>C
ENST00000614526.1:c.-223+431T>C	ENSP00000480814.1:n.-223+431T>C
NM_001098268.1:c.-29+3109T>C	NP_001091738.1:n.-29+3109T>C
NM_206937.1:c.-102+431T>C	NP_996820.1:n.-102+431T>C
XM_005254056.1:c.-78+431T>C	XP_005254113.1:n.-78+431T>C
XM_005254057.3:c.-210+271T>C	XP_005254114.1:n.-210+271T>C
XM_005254058.2:c.-29+431T>C	XP_005254115.1:n.-29+431T>C
XM_006719951.2:c.-209-335T>C	XP_006720014.1:n.-209-335T>C
XM_006719952.1:c.-185-335T>C	XP_006720015.1:n.-185-335T>C
XM_011521091.1:c.-209-335T>C	XP_011519393.1:n.-209-335T>C
XM_011521092.1:c.-102+271T>C	XP_011519394.1:n.-102+271T>C
NM_001330595.1:c.-223+431T>C	NP_001317524.1:n.-223+431T>C
NM_001352598.1:c.-185-335T>C	NP_001339527.1:n.-185-335T>C
NM_001352599.1:c.-209-335T>C	NP_001339528.1:n.-209-335T>C
NM_001352600.1:c.-102+431T>C	NP_001339529.1:n.-102+431T>C
NM_001352601.1:c.-210+271T>C	NP_001339530.1:n.-210+271T>C
NM_001352602.1:c.-102+271T>C	NP_001339531.1:n.-102+271T>C
NM_001352603.1:c.-102+226T>C	NP_001339532.1:n.-102+226T>C
NM_001352604.1:c.-94+271T>C	NP_001339533.1:n.-94+271T>C
XM_005254058.4:c.-29+431T>C	XP_005254115.1:n.-29+431T>C
XM_006719951.3:c.-209-335T>C	XP_006720014.1:n.-209-335T>C
XM_017020565.1:c.-93-335T>C	XP_016876054.1:n.-93-335T>C
XM_017020566.1:c.-93-335T>C	XP_016876055.1:n.-93-335T>C
XM_017020568.2:c.-93-335T>C	XP_016876057.1:n.-93-335T>C
XM_017020571.1:c.-185-335T>C	XP_016876060.1:n.-185-335T>C
XM_017020573.1:c.-223+271T>C	XP_016876062.1:n.-223+271T>C
NM_001098268.2:c.-29+3109T>C	NP_001091738.1:n.-29+3109T>C
NM_001352598.2:c.-185-335T>C	NP_001339527.1:n.-185-335T>C
NM_001352599.2:c.-209-335T>C	NP_001339528.1:n.-209-335T>C
NM_001352600.2:c.-102+431T>C	NP_001339529.1:n.-102+431T>C
NM_001352601.2:c.-210+271T>C	NP_001339530.1:n.-210+271T>C
NM_001352602.2:c.-102+271T>C	NP_001339531.1:n.-102+271T>C
NM_206937.2:c.-102+431T>C MANE Select	NP_996820.1:n.-102+431T>C
NM_001330595.2:c.-223+431T>C	NP_001317524.1:n.-223+431T>C
NM_001352604.2:c.-94+271T>C	NP_001339533.1:n.-94+271T>C
NM_001379095.1:c.-298-246T>C	NP_001366024.1:n.-298-246T>C