Canonical Allele Identifier: CA348391515

Gene: ERCC3

Linked Data

• MyVariant Identifiers: chr2:g.128050214A>T (hg19) ; chr2:g.127292638A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127292638A>T , CM000664.2:g.127292638A>T	GRCh38
NC_000002.11:g.128050214A>T , CM000664.1:g.128050214A>T	GRCh37
NC_000002.10:g.127766684A>T	NCBI36
NG_007454.1:g.6539T>A , LRG_462:g.6539T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000285398.7:c.443T>A MANE Select	ENSP00000285398.2:p.Val148Asp
ENST00000642308.1:c.443T>A	ENSP00000496684.1:p.Val148Asp
ENST00000644317.1:c.301T>A	ENSP00000494012.1:p.Ser101Thr
ENST00000645233.1:c.443T>A	ENSP00000494116.1:p.Val148Asp
ENST00000645467.1:c.443T>A	ENSP00000494889.1:p.Val148Asp
ENST00000645736.1:c.299T>A	ENSP00000494545.1:p.Val100Asp
ENST00000646654.1:c.443T>A	ENSP00000494526.1:p.Val148Asp
ENST00000647169.1:c.443T>A	ENSP00000495619.1:p.Val148Asp
ENST00000647496.1:c.16T>A
ENST00000285398.6:c.443T>A	ENSP00000285398.2:p.Val148Asp
ENST00000426778.5:c.*424T>A	ENSP00000415335.1:n.*424T>A
ENST00000445889.5:c.*486T>A	ENSP00000390888.1:n.*486T>A
ENST00000462306.5:n.357T>A
ENST00000490062.1:n.373T>A
ENST00000494464.5:n.327T>A
NM_000122.1:c.443T>A , LRG_462t1:c.443T>A	NP_000113.1:p.Val148Asp
NM_001303416.1:c.251T>A	NP_001290345.1:p.Val84Asp
NM_001303418.1:c.251T>A	NP_001290347.1:p.Val84Asp
XM_011510794.1:c.443T>A	XP_011509096.1:p.Val148Asp
XM_011510795.1:c.-14T>A	XP_011509097.1:n.-14T>A
XM_011510794.2:c.443T>A	XP_011509096.1:p.Val148Asp
XM_017003583.1:c.-14T>A	XP_016859072.1:n.-14T>A
NM_000122.2:c.443T>A MANE Select	NP_000113.1:p.Val148Asp
NM_001303416.2:c.251T>A	NP_001290345.1:p.Val84Asp
NM_001303418.2:c.251T>A	NP_001290347.1:p.Val84Asp