Canonical Allele Identifier: CA348391970
Community Standard Title: NM_000122.2(ERCC3):c.235-1G>A
Gene: ERCC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127292847C>T , CM000664.2:g.127292847C>T GRCh38
NC_000002.11:g.128050423C>T , CM000664.1:g.128050423C>T GRCh37
NC_000002.10:g.127766893C>T NCBI36
NG_007454.1:g.6330G>A , LRG_462:g.6330G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000122.2:c.235-1G>A MANE Select NP_000113.1:n.235-1G>A
ENST00000285398.7:c.235-1G>A MANE Select ENSP00000285398.2:n.235-1G>A
NM_000122.1:c.235-1G>A , LRG_462t1:c.235-1G>A NP_000113.1:n.235-1G>A
NM_001303416.1:c.43-1G>A NP_001290345.1:n.43-1G>A
NM_001303416.2:c.43-1G>A NP_001290345.1:n.43-1G>A
NM_001303418.1:c.43-1G>A NP_001290347.1:n.43-1G>A
NM_001303418.2:c.43-1G>A NP_001290347.1:n.43-1G>A
ENST00000285398.6:c.235-1G>A ENSP00000285398.2:n.235-1G>A
ENST00000426778.5:c.*216-1G>A ENSP00000415335.1:n.*216-1G>A
ENST00000445889.5:c.*278-1G>A ENSP00000390888.1:n.*278-1G>A
ENST00000462306.5:n.291-143G>A
ENST00000490062.1:n.307-143G>A
ENST00000494464.5:n.261-143G>A
ENST00000642308.1:c.235-1G>A ENSP00000496684.1:n.235-1G>A
ENST00000644317.1:c.235-143G>A ENSP00000494012.1:n.235-143G>A
ENST00000645233.1:c.235-1G>A ENSP00000494116.1:n.235-1G>A
ENST00000645467.1:c.235-1G>A ENSP00000494889.1:n.235-1G>A
ENST00000645736.1:c.91-1G>A ENSP00000494545.1:n.91-1G>A
ENST00000646654.1:c.235-1G>A ENSP00000494526.1:n.235-1G>A
ENST00000647169.1:c.235-1G>A ENSP00000495619.1:n.235-1G>A
XM_011510794.1:c.235-1G>A XP_011509096.1:n.235-1G>A
XM_011510794.2:c.235-1G>A XP_011509096.1:n.235-1G>A
XM_011510795.1:c.-80-143G>A XP_011509097.1:n.-80-143G>A
XM_017003583.1:c.-80-143G>A XP_016859072.1:n.-80-143G>A