Canonical Allele Identifier: CA14707570

Gene: LIG1

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48128151C>T , CM000681.2:g.48128151C>T	GRCh38
NC_000019.9:g.48631408C>T , CM000681.1:g.48631408C>T	GRCh37
NC_000019.8:g.53323220C>T	NCBI36
NG_007395.1:g.47153G>A , LRG_78:g.47153G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000596549.6:c.1618-131G>A	ENSP00000471861.2:n.1618-131G>A
ENST00000596672.6:c.*880-131G>A	ENSP00000472331.2:n.*880-131G>A
ENST00000597901.2:n.2501-131G>A
ENST00000699866.1:c.1819-131G>A	ENSP00000514663.1:n.1819-131G>A
ENST00000699867.1:n.1839-131G>A
ENST00000699868.1:c.1822-131G>A	ENSP00000514664.1:n.1822-131G>A
ENST00000699869.1:c.*146-131G>A	ENSP00000514665.1:n.*146-131G>A
ENST00000699870.1:c.*146-131G>A	ENSP00000514666.1:n.*146-131G>A
ENST00000699871.1:c.1723-131G>A	ENSP00000514667.1:n.1723-131G>A
ENST00000699872.1:c.*1591-131G>A	ENSP00000514668.1:n.*1591-131G>A
ENST00000699873.1:c.1732-131G>A	ENSP00000514669.1:n.1732-131G>A
ENST00000699874.1:c.1732-131G>A	ENSP00000514670.1:n.1732-131G>A
ENST00000699875.1:c.1819-131G>A	ENSP00000514671.1:n.1819-131G>A
ENST00000699876.1:n.2190-131G>A
ENST00000699877.1:c.1819-131G>A	ENSP00000514672.1:n.1819-131G>A
ENST00000699878.1:c.*316-131G>A	ENSP00000514673.1:n.*316-131G>A
ENST00000699879.1:n.1980-131G>A
ENST00000263274.12:c.1822-131G>A MANE Select	ENSP00000263274.6:n.1822-131G>A
ENST00000263274.11:c.1822-131G>A	ENSP00000263274.6:n.1822-131G>A
ENST00000427526.6:c.1729-131G>A	ENSP00000442841.1:n.1729-131G>A
ENST00000536218.5:c.1618-131G>A	ENSP00000441531.1:n.1618-131G>A
ENST00000594067.5:n.1578-131G>A
ENST00000594759.5:c.1819-131G>A	ENSP00000471380.1:n.1819-131G>A
ENST00000596457.1:n.610-131G>A
ENST00000596672.5:c.256-131G>A
ENST00000601091.5:c.1822-131G>A	ENSP00000471836.1:n.1822-131G>A
ENST00000613670.4:c.1822-131G>A	ENSP00000483027.1:n.1822-131G>A
NM_000234.2:c.1822-131G>A	NP_000225.1:n.1822-131G>A
NM_001289063.1:c.1729-131G>A	NP_001275992.1:n.1729-131G>A
NM_001289064.1:c.1618-131G>A	NP_001275993.1:n.1618-131G>A
NR_110296.1:n.2239-131G>A
XM_005258934.2:c.1732-131G>A	XP_005258991.1:n.1732-131G>A
XM_006723215.2:c.1819-131G>A	XP_006723278.1:n.1819-131G>A
XM_006723216.2:c.1822-131G>A	XP_006723279.1:n.1822-131G>A
XR_243932.2:n.1879-131G>A
XR_430200.1:n.1793-131G>A
NM_001320970.1:c.1819-131G>A	NP_001307899.1:n.1819-131G>A
NM_001320971.1:c.1732-131G>A	NP_001307900.1:n.1732-131G>A
NR_135497.1:n.2242-131G>A
NR_135498.1:n.2071-131G>A
NR_135499.1:n.2152-131G>A
NR_135500.1:n.2419-131G>A
NR_135501.1:n.2063-131G>A
XM_024451513.1:c.1714-131G>A	XP_024307281.1:n.1714-131G>A
XR_002958315.1:n.2148-131G>A
XR_002958316.1:n.2040-131G>A
NM_000234.3:c.1822-131G>A MANE Select	NP_000225.1:n.1822-131G>A
NM_001289063.2:c.1729-131G>A	NP_001275992.1:n.1729-131G>A
NM_001320970.2:c.1819-131G>A	NP_001307899.1:n.1819-131G>A
NM_001320971.2:c.1732-131G>A	NP_001307900.1:n.1732-131G>A
NR_110296.2:n.1980-131G>A
NR_135497.2:n.1983-131G>A
NR_135498.2:n.1812-131G>A
NR_135499.2:n.1893-131G>A
NR_135500.2:n.2160-131G>A
NR_135501.2:n.1804-131G>A
NM_001289064.2:c.1618-131G>A	NP_001275993.1:n.1618-131G>A