Canonical Allele Identifier: CA2209081392
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13944703G= , CM000678.2:g.13944703G= GRCh38
NC_000016.9:g.14038560G= , CM000678.1:g.14038560G= GRCh37
NC_000016.8:g.13946061G= NCBI36
NG_011442.1:g.29547G= , LRG_463:g.29547G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2043-20G= ENSP00000507912.1:n.2043-20G=
ENST00000683962.1:c.*1599-20G= ENSP00000506854.1:n.*1599-20G=
ENST00000311895.8:c.1905-20G= MANE Select ENSP00000310520.7:n.1905-20G=
ENST00000311895.7:c.1905-20G= ENSP00000310520.7:n.1905-20G=
ENST00000389138.7:n.1182-20G=
ENST00000462862.1:c.218-20G= ENSP00000461322.1:n.218-20G=
NM_005236.2:c.1905-20G= , LRG_463t1:c.1905-20G= NP_005227.1:n.1905-20G=
XM_011522424.1:c.2043-20G= XP_011520726.1:n.2043-20G=
XM_011522425.1:c.1362-20G= XP_011520727.1:n.1362-20G=
XM_011522426.1:c.1116-20G= XP_011520728.1:n.1116-20G=
XM_011522427.1:c.555-20G= XP_011520729.1:n.555-20G=
XR_932805.1:n.2064-20G=
XM_011522424.3:c.2043-20G= XP_011520726.1:n.2043-20G=
XM_017023043.2:c.1116-20G= XP_016878532.1:n.1116-20G=
NM_005236.3:c.1905-20G= MANE Select NP_005227.1:n.1905-20G=