Canonical Allele Identifier: CA2660987381

Gene: ERCC3

Linked Data

• gnomAD v4: 2-127292727-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127292728dup , CM000664.2:g.127292728dup	GRCh38
NC_000002.11:g.128050304dup , CM000664.1:g.128050304dup	GRCh37
NC_000002.10:g.127766774dup	NCBI36
NG_007454.1:g.6449dup , LRG_462:g.6449dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000285398.7:c.353dup MANE Select	ENSP00000285398.2:p.Thr119AsnfsTer17
ENST00000642308.1:c.353dup	ENSP00000496684.1:p.Thr119AsnfsTer17
ENST00000644317.1:c.235-24dup	ENSP00000494012.1:n.235-24dup
ENST00000645233.1:c.353dup	ENSP00000494116.1:p.Thr119AsnfsTer17
ENST00000645467.1:c.353dup	ENSP00000494889.1:p.Thr119AsnfsTer17
ENST00000645736.1:c.209dup	ENSP00000494545.1:p.Thr71AsnfsTer17
ENST00000646654.1:c.353dup	ENSP00000494526.1:p.Thr119AsnfsTer17
ENST00000647169.1:c.353dup	ENSP00000495619.1:p.Thr119AsnfsTer17
ENST00000285398.6:c.353dup	ENSP00000285398.2:p.Thr119AsnfsTer17
ENST00000426778.5:c.*334dup	ENSP00000415335.1:n.*334dup
ENST00000445889.5:c.*396dup	ENSP00000390888.1:n.*396dup
ENST00000462306.5:n.291-24dup
ENST00000490062.1:n.307-24dup
ENST00000494464.5:n.261-24dup
NM_000122.1:c.353dup , LRG_462t1:c.353dup	NP_000113.1:p.Thr119AsnfsTer17
NM_001303416.1:c.161dup	NP_001290345.1:p.Thr55AsnfsTer17
NM_001303418.1:c.161dup	NP_001290347.1:p.Thr55AsnfsTer17
XM_011510794.1:c.353dup	XP_011509096.1:p.Thr119AsnfsTer17
XM_011510795.1:c.-80-24dup	XP_011509097.1:n.-80-24dup
XM_011510794.2:c.353dup	XP_011509096.1:p.Thr119AsnfsTer17
XM_017003583.1:c.-80-24dup	XP_016859072.1:n.-80-24dup
NM_000122.2:c.353dup MANE Select	NP_000113.1:p.Thr119AsnfsTer17
NM_001303416.2:c.161dup	NP_001290345.1:p.Thr55AsnfsTer17
NM_001303418.2:c.161dup	NP_001290347.1:p.Thr55AsnfsTer17