Canonical Allele Identifier: CA2209082724
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13947814C= , CM000678.2:g.13947814C= GRCh38
NC_000016.9:g.14041671C= , CM000678.1:g.14041671C= GRCh37
NC_000016.8:g.13949172C= NCBI36
NG_011442.1:g.32658C= , LRG_463:g.32658C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2356C= ENSP00000507912.1:p.Arg786=
ENST00000683962.1:c.*1912C= ENSP00000506854.1:n.*1912C=
ENST00000311895.8:c.2218C= MANE Select ENSP00000310520.7:p.Arg740=
ENST00000311895.7:c.2218C= ENSP00000310520.7:p.Arg740=
ENST00000389138.7:n.1495C=
ENST00000462862.1:c.531C= ENSP00000461322.1:n.531C=
NM_005236.2:c.2218C= , LRG_463t1:c.2218C= NP_005227.1:p.Arg740=
XM_011522424.1:c.2356C= XP_011520726.1:p.Arg786=
XM_011522425.1:c.1675C= XP_011520727.1:p.Arg559=
XM_011522426.1:c.1429C= XP_011520728.1:p.Arg477=
XM_011522427.1:c.868C= XP_011520729.1:p.Arg290=
XR_932805.1:n.2377C=
XM_011522424.3:c.2356C= XP_011520726.1:p.Arg786=
XM_017023043.2:c.1429C= XP_016878532.1:p.Arg477=
NM_005236.3:c.2218C= MANE Select NP_005227.1:p.Arg740=