Canonical Allele Identifier: CA7910710
Gene: ERCC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 941684
dbSNP Id: rs374978891

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13947844C>T , CM000678.2:g.13947844C>T GRCh38
NC_000016.9:g.14041701C>T , CM000678.1:g.14041701C>T GRCh37
NC_000016.8:g.13949202C>T NCBI36
NG_011442.1:g.32688C>T , LRG_463:g.32688C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682617.1:c.2386C>T ENSP00000507912.1:p.Arg796Cys
ENST00000683962.1:c.*1942C>T ENSP00000506854.1:n.*1942C>T
ENST00000311895.8:c.2248C>T MANE Select ENSP00000310520.7:p.Arg750Cys
ENST00000311895.7:c.2248C>T ENSP00000310520.7:p.Arg750Cys
ENST00000389138.7:n.1525C>T
ENST00000462862.1:c.561C>T ENSP00000461322.1:n.561C>T
NM_005236.2:c.2248C>T , LRG_463t1:c.2248C>T NP_005227.1:p.Arg750Cys
XM_011522424.1:c.2386C>T XP_011520726.1:p.Arg796Cys
XM_011522425.1:c.1705C>T XP_011520727.1:p.Arg569Cys
XM_011522426.1:c.1459C>T XP_011520728.1:p.Arg487Cys
XM_011522427.1:c.898C>T XP_011520729.1:p.Arg300Cys
XR_932805.1:n.2407C>T
XM_011522424.3:c.2386C>T XP_011520726.1:p.Arg796Cys
XM_017023043.2:c.1459C>T XP_016878532.1:p.Arg487Cys
NM_005236.3:c.2248C>T MANE Select NP_005227.1:p.Arg750Cys