Canonical Allele Identifier: CA2209082819
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948003T= , CM000678.2:g.13948003T= GRCh38
NC_000016.9:g.14041860T= , CM000678.1:g.14041860T= GRCh37
NC_000016.8:g.13949361T= NCBI36
NG_011442.1:g.32847T= , LRG_463:g.32847T=

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2545T= ENSP00000507912.1:p.Cys849=
ENST00000683962.1:c.*2101T= ENSP00000506854.1:n.*2101T=
ENST00000311895.8:c.2407T= MANE Select ENSP00000310520.7:p.Cys803=
ENST00000311895.7:c.2407T= ENSP00000310520.7:p.Cys803=
ENST00000389138.7:n.1684T=
ENST00000462862.1:c.720T= ENSP00000461322.1:n.720T=
NM_005236.2:c.2407T= , LRG_463t1:c.2407T= NP_005227.1:p.Cys803=
XM_011522424.1:c.2545T= XP_011520726.1:p.Cys849=
XM_011522425.1:c.1864T= XP_011520727.1:p.Cys622=
XM_011522426.1:c.1618T= XP_011520728.1:p.Cys540=
XM_011522427.1:c.1057T= XP_011520729.1:p.Cys353=
XR_932805.1:n.2566T=
XM_011522424.3:c.2545T= XP_011520726.1:p.Cys849=
XM_017023043.2:c.1618T= XP_016878532.1:p.Cys540=
NM_005236.3:c.2407T= MANE Select NP_005227.1:p.Cys803=