Canonical Allele Identifier: CA348391456

Gene: ERCC3

Linked Data

• MyVariant Identifiers: chr2:g.128050189A>C (hg19) ; chr2:g.127292613A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127292613A>C , CM000664.2:g.127292613A>C	GRCh38
NC_000002.11:g.128050189A>C , CM000664.1:g.128050189A>C	GRCh37
NC_000002.10:g.127766659A>C	NCBI36
NG_007454.1:g.6564T>G , LRG_462:g.6564T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285398.7:c.468T>G MANE Select	ENSP00000285398.2:p.Ile156Met
ENST00000642308.1:c.468T>G	ENSP00000496684.1:p.Ile156Met
ENST00000644317.1:c.326T>G	ENSP00000494012.1:p.Leu109Ter
ENST00000645233.1:c.468T>G	ENSP00000494116.1:p.Ile156Met
ENST00000645467.1:c.468T>G	ENSP00000494889.1:p.Ile156Met
ENST00000645736.1:c.324T>G	ENSP00000494545.1:p.Ile108Met
ENST00000646654.1:c.468T>G	ENSP00000494526.1:p.Ile156Met
ENST00000647169.1:c.468T>G	ENSP00000495619.1:p.Ile156Met
ENST00000647496.1:c.41T>G
ENST00000285398.6:c.468T>G	ENSP00000285398.2:p.Ile156Met
ENST00000426778.5:c.*449T>G	ENSP00000415335.1:n.*449T>G
ENST00000445889.5:c.*511T>G	ENSP00000390888.1:n.*511T>G
ENST00000462306.5:n.382T>G
ENST00000490062.1:n.398T>G
ENST00000494464.5:n.352T>G
NM_000122.1:c.468T>G , LRG_462t1:c.468T>G	NP_000113.1:p.Ile156Met
NM_001303416.1:c.276T>G	NP_001290345.1:p.Ile92Met
NM_001303418.1:c.276T>G	NP_001290347.1:p.Ile92Met
XM_011510794.1:c.468T>G	XP_011509096.1:p.Ile156Met
XM_011510795.1:c.12T>G	XP_011509097.1:p.Ile4Met
XM_011510794.2:c.468T>G	XP_011509096.1:p.Ile156Met
XM_017003583.1:c.12T>G	XP_016859072.1:p.Ile4Met
NM_000122.2:c.468T>G MANE Select	NP_000113.1:p.Ile156Met
NM_001303416.2:c.276T>G	NP_001290345.1:p.Ile92Met
NM_001303418.2:c.276T>G	NP_001290347.1:p.Ile92Met