Canonical Allele Identifier: CA2209081564

Gene: ERCC4

Linked Data

• dbSNP Id: rs2032489960

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13945076del , CM000678.2:g.13945076del	GRCh38
NC_000016.9:g.14038933del , CM000678.1:g.14038933del	GRCh37
NC_000016.8:g.13946434del	NCBI36
NG_011442.1:g.29920del , LRG_463:g.29920del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2155+241del	ENSP00000507912.1:n.2155+241del
ENST00000683962.1:c.*1711+241del	ENSP00000506854.1:n.*1711+241del
ENST00000311895.8:c.2017+241del MANE Select	ENSP00000310520.7:n.2017+241del
ENST00000311895.7:c.2017+241del	ENSP00000310520.7:n.2017+241del
ENST00000389138.7:n.1294+241del
ENST00000462862.1:c.330+241del	ENSP00000461322.1:n.330+241del
NM_005236.2:c.2017+241del , LRG_463t1:c.2017+241del	NP_005227.1:n.2017+241del
XM_011522424.1:c.2155+241del	XP_011520726.1:n.2155+241del
XM_011522425.1:c.1474+241del	XP_011520727.1:n.1474+241del
XM_011522426.1:c.1228+241del	XP_011520728.1:n.1228+241del
XM_011522427.1:c.667+241del	XP_011520729.1:n.667+241del
XR_932805.1:n.2176+241del
XM_011522424.3:c.2155+241del	XP_011520726.1:n.2155+241del
XM_017023043.2:c.1228+241del	XP_016878532.1:n.1228+241del
NM_005236.3:c.2017+241del MANE Select	NP_005227.1:n.2017+241del