Canonical Allele Identifier: CA2631831445
Gene: ERCC4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948406dup , CM000678.2:g.13948406dup GRCh38
NC_000016.9:g.14042263dup , CM000678.1:g.14042263dup GRCh37
NC_000016.8:g.13949764dup NCBI36
NG_011442.1:g.33250dup , LRG_463:g.33250dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000682617.1:c.*59dup ENSP00000507912.1:n.*59dup
ENST00000683962.1:c.*2504dup ENSP00000506854.1:n.*2504dup
ENST00000311895.8:c.*59dup MANE Select ENSP00000310520.7:n.*59dup
ENST00000311895.7:c.*59dup ENSP00000310520.7:n.*59dup
ENST00000389138.7:n.2087dup
NM_005236.2:c.*59dup , LRG_463t1:c.*59dup NP_005227.1:n.*59dup
XM_011522424.1:c.*59dup XP_011520726.1:n.*59dup
XM_011522425.1:c.*59dup XP_011520727.1:n.*59dup
XM_011522426.1:c.*59dup XP_011520728.1:n.*59dup
XM_011522427.1:c.*59dup XP_011520729.1:n.*59dup
XR_932805.1:n.2969dup
XM_011522424.3:c.*59dup XP_011520726.1:n.*59dup
XM_017023043.2:c.*59dup XP_016878532.1:n.*59dup
NM_005236.3:c.*59dup MANE Select NP_005227.1:n.*59dup