Canonical Allele Identifier: CA919662886

Gene: ERCC4

Linked Data

• dbSNP Id: rs1596633966

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13944667_13944671del , CM000678.2:g.13944667_13944671del	GRCh38
NC_000016.9:g.14038524_14038528del , CM000678.1:g.14038524_14038528del	GRCh37
NC_000016.8:g.13946025_13946029del	NCBI36
NG_011442.1:g.29511_29515del , LRG_463:g.29511_29515del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2043-56_2043-52del	ENSP00000507912.1:n.2043-56_2043-52del
ENST00000683962.1:c.*1599-56_*1599-52del	ENSP00000506854.1:n.*1599-56_*1599-52del
ENST00000311895.8:c.1905-56_1905-52del MANE Select	ENSP00000310520.7:n.1905-56_1905-52del
ENST00000311895.7:c.1905-56_1905-52del	ENSP00000310520.7:n.1905-56_1905-52del
ENST00000389138.7:n.1182-56_1182-52del
ENST00000462862.1:c.218-56_218-52del	ENSP00000461322.1:n.218-56_218-52del
NM_005236.2:c.1905-56_1905-52del , LRG_463t1:c.1905-56_1905-52del	NP_005227.1:n.1905-56_1905-52del
XM_011522424.1:c.2043-56_2043-52del	XP_011520726.1:n.2043-56_2043-52del
XM_011522425.1:c.1362-56_1362-52del	XP_011520727.1:n.1362-56_1362-52del
XM_011522426.1:c.1116-56_1116-52del	XP_011520728.1:n.1116-56_1116-52del
XM_011522427.1:c.555-56_555-52del	XP_011520729.1:n.555-56_555-52del
XR_932805.1:n.2064-56_2064-52del
XM_011522424.3:c.2043-56_2043-52del	XP_011520726.1:n.2043-56_2043-52del
XM_017023043.2:c.1116-56_1116-52del	XP_016878532.1:n.1116-56_1116-52del
NM_005236.3:c.1905-56_1905-52del MANE Select	NP_005227.1:n.1905-56_1905-52del