Canonical Allele Identifier: CA2209082845
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948055A= , CM000678.2:g.13948055A= GRCh38
NC_000016.9:g.14041912A= , CM000678.1:g.14041912A= GRCh37
NC_000016.8:g.13949413A= NCBI36
NG_011442.1:g.32899A= , LRG_463:g.32899A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682617.1:c.2597A= ENSP00000507912.1:p.Lys866=
ENST00000683962.1:c.*2153A= ENSP00000506854.1:n.*2153A=
ENST00000311895.8:c.2459A= MANE Select ENSP00000310520.7:p.Lys820=
ENST00000311895.7:c.2459A= ENSP00000310520.7:p.Lys820=
ENST00000389138.7:n.1736A=
NM_005236.2:c.2459A= , LRG_463t1:c.2459A= NP_005227.1:p.Lys820=
XM_011522424.1:c.2597A= XP_011520726.1:p.Lys866=
XM_011522425.1:c.1916A= XP_011520727.1:p.Lys639=
XM_011522426.1:c.1670A= XP_011520728.1:p.Lys557=
XM_011522427.1:c.1109A= XP_011520729.1:p.Lys370=
XR_932805.1:n.2618A=
XM_011522424.3:c.2597A= XP_011520726.1:p.Lys866=
XM_017023043.2:c.1670A= XP_016878532.1:p.Lys557=
NM_005236.3:c.2459A= MANE Select NP_005227.1:p.Lys820=