Canonical Allele Identifier: CA656808150

Gene: ERCC4

Linked Data

• COSMIC: COSN21806216

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948500_13948501insT , CM000678.2:g.13948500_13948501insT	GRCh38
NC_000016.9:g.14042357_14042358insT , CM000678.1:g.14042357_14042358insT	GRCh37
NC_000016.8:g.13949858_13949859insT	NCBI36
NG_011442.1:g.33344_33345insT , LRG_463:g.33344_33345insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.*153_*154insT	ENSP00000507912.1:n.*153_*154insT
ENST00000683962.1:c.*2598_*2599insT	ENSP00000506854.1:n.*2598_*2599insT
ENST00000311895.8:c.*153_*154insT MANE Select	ENSP00000310520.7:n.*153_*154insT
ENST00000311895.7:c.*153_*154insT	ENSP00000310520.7:n.*153_*154insT
NM_005236.2:c.*153_*154insT , LRG_463t1:c.*153_*154insT	NP_005227.1:n.*153_*154insT
XM_011522424.1:c.*153_*154insT	XP_011520726.1:n.*153_*154insT
XM_011522425.1:c.*153_*154insT	XP_011520727.1:n.*153_*154insT
XM_011522426.1:c.*153_*154insT	XP_011520728.1:n.*153_*154insT
XM_011522427.1:c.*153_*154insT	XP_011520729.1:n.*153_*154insT
XR_932805.1:n.3063_3064insT
XM_011522424.3:c.*153_*154insT	XP_011520726.1:n.*153_*154insT
XM_017023043.2:c.*153_*154insT	XP_016878532.1:n.*153_*154insT
NM_005236.3:c.*153_*154insT MANE Select	NP_005227.1:n.*153_*154insT