Canonical Allele Identifier: CA348391517

Gene: ERCC3

Linked Data

• MyVariant Identifiers: chr2:g.128050215C>G (hg19) ; chr2:g.127292639C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127292639C>G , CM000664.2:g.127292639C>G	GRCh38
NC_000002.11:g.128050215C>G , CM000664.1:g.128050215C>G	GRCh37
NC_000002.10:g.127766685C>G	NCBI36
NG_007454.1:g.6538G>C , LRG_462:g.6538G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000285398.7:c.442G>C MANE Select	ENSP00000285398.2:p.Val148Leu
ENST00000642308.1:c.442G>C	ENSP00000496684.1:p.Val148Leu
ENST00000644317.1:c.300G>C	ENSP00000494012.1:p.Glu100Asp
ENST00000645233.1:c.442G>C	ENSP00000494116.1:p.Val148Leu
ENST00000645467.1:c.442G>C	ENSP00000494889.1:p.Val148Leu
ENST00000645736.1:c.298G>C	ENSP00000494545.1:p.Val100Leu
ENST00000646654.1:c.442G>C	ENSP00000494526.1:p.Val148Leu
ENST00000647169.1:c.442G>C	ENSP00000495619.1:p.Val148Leu
ENST00000647496.1:c.15G>C
ENST00000285398.6:c.442G>C	ENSP00000285398.2:p.Val148Leu
ENST00000426778.5:c.*423G>C	ENSP00000415335.1:n.*423G>C
ENST00000445889.5:c.*485G>C	ENSP00000390888.1:n.*485G>C
ENST00000462306.5:n.356G>C
ENST00000490062.1:n.372G>C
ENST00000494464.5:n.326G>C
NM_000122.1:c.442G>C , LRG_462t1:c.442G>C	NP_000113.1:p.Val148Leu
NM_001303416.1:c.250G>C	NP_001290345.1:p.Val84Leu
NM_001303418.1:c.250G>C	NP_001290347.1:p.Val84Leu
XM_011510794.1:c.442G>C	XP_011509096.1:p.Val148Leu
XM_011510795.1:c.-15G>C	XP_011509097.1:n.-15G>C
XM_011510794.2:c.442G>C	XP_011509096.1:p.Val148Leu
XM_017003583.1:c.-15G>C	XP_016859072.1:n.-15G>C
NM_000122.2:c.442G>C MANE Select	NP_000113.1:p.Val148Leu
NM_001303416.2:c.250G>C	NP_001290345.1:p.Val84Leu
NM_001303418.2:c.250G>C	NP_001290347.1:p.Val84Leu