Canonical Allele Identifier: CA2209081399
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13944722G= , CM000678.2:g.13944722G= GRCh38
NC_000016.9:g.14038579G= , CM000678.1:g.14038579G= GRCh37
NC_000016.8:g.13946080G= NCBI36
NG_011442.1:g.29566G= , LRG_463:g.29566G=

Transcript Alleles

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