Canonical Allele Identifier: CA2209082820
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948005C= , CM000678.2:g.13948005C= GRCh38
NC_000016.9:g.14041862C= , CM000678.1:g.14041862C= GRCh37
NC_000016.8:g.13949363C= NCBI36
NG_011442.1:g.32849C= , LRG_463:g.32849C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2547C= ENSP00000507912.1:p.Cys849=
ENST00000683962.1:c.*2103C= ENSP00000506854.1:n.*2103C=
ENST00000311895.8:c.2409C= MANE Select ENSP00000310520.7:p.Cys803=
ENST00000311895.7:c.2409C= ENSP00000310520.7:p.Cys803=
ENST00000389138.7:n.1686C=
NM_005236.2:c.2409C= , LRG_463t1:c.2409C= NP_005227.1:p.Cys803=
XM_011522424.1:c.2547C= XP_011520726.1:p.Cys849=
XM_011522425.1:c.1866C= XP_011520727.1:p.Cys622=
XM_011522426.1:c.1620C= XP_011520728.1:p.Cys540=
XM_011522427.1:c.1059C= XP_011520729.1:p.Cys353=
XR_932805.1:n.2568C=
XM_011522424.3:c.2547C= XP_011520726.1:p.Cys849=
XM_017023043.2:c.1620C= XP_016878532.1:p.Cys540=
NM_005236.3:c.2409C= MANE Select NP_005227.1:p.Cys803=