Canonical Allele Identifier: CA394822783
Gene: ERCC4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13947874G>A , CM000678.2:g.13947874G>A GRCh38
NC_000016.9:g.14041731G>A , CM000678.1:g.14041731G>A GRCh37
NC_000016.8:g.13949232G>A NCBI36
NG_011442.1:g.32718G>A , LRG_463:g.32718G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2416G>A ENSP00000507912.1:p.Glu806Lys
ENST00000683962.1:c.*1972G>A ENSP00000506854.1:n.*1972G>A
ENST00000311895.8:c.2278G>A MANE Select ENSP00000310520.7:p.Glu760Lys
ENST00000311895.7:c.2278G>A ENSP00000310520.7:p.Glu760Lys
ENST00000389138.7:n.1555G>A
ENST00000462862.1:c.591G>A ENSP00000461322.1:n.591G>A
NM_005236.2:c.2278G>A , LRG_463t1:c.2278G>A NP_005227.1:p.Glu760Lys
XM_011522424.1:c.2416G>A XP_011520726.1:p.Glu806Lys
XM_011522425.1:c.1735G>A XP_011520727.1:p.Glu579Lys
XM_011522426.1:c.1489G>A XP_011520728.1:p.Glu497Lys
XM_011522427.1:c.928G>A XP_011520729.1:p.Glu310Lys
XR_932805.1:n.2437G>A
XM_011522424.3:c.2416G>A XP_011520726.1:p.Glu806Lys
XM_017023043.2:c.1489G>A XP_016878532.1:p.Glu497Lys
NM_005236.3:c.2278G>A MANE Select NP_005227.1:p.Glu760Lys