Canonical Allele Identifier: CA2209082879
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948141C= , CM000678.2:g.13948141C= GRCh38
NC_000016.9:g.14041998C= , CM000678.1:g.14041998C= GRCh37
NC_000016.8:g.13949499C= NCBI36
NG_011442.1:g.32985C= , LRG_463:g.32985C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2683C= ENSP00000507912.1:p.Gln895=
ENST00000683962.1:c.*2239C= ENSP00000506854.1:n.*2239C=
ENST00000311895.8:c.2545C= MANE Select ENSP00000310520.7:p.Gln849=
ENST00000311895.7:c.2545C= ENSP00000310520.7:p.Gln849=
ENST00000389138.7:n.1822C=
NM_005236.2:c.2545C= , LRG_463t1:c.2545C= NP_005227.1:p.Gln849=
XM_011522424.1:c.2683C= XP_011520726.1:p.Gln895=
XM_011522425.1:c.2002C= XP_011520727.1:p.Gln668=
XM_011522426.1:c.1756C= XP_011520728.1:p.Gln586=
XM_011522427.1:c.1195C= XP_011520729.1:p.Gln399=
XR_932805.1:n.2704C=
XM_011522424.3:c.2683C= XP_011520726.1:p.Gln895=
XM_017023043.2:c.1756C= XP_016878532.1:p.Gln586=
NM_005236.3:c.2545C= MANE Select NP_005227.1:p.Gln849=