Canonical Allele Identifier: CA2631831563

Gene: ERCC4

Linked Data

• gnomAD v4: 16-13948558-ACCGTC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948559_13948563del , CM000678.2:g.13948559_13948563del	GRCh38
NC_000016.9:g.14042416_14042420del , CM000678.1:g.14042416_14042420del	GRCh37
NC_000016.8:g.13949917_13949921del	NCBI36
NG_011442.1:g.33403_33407del , LRG_463:g.33403_33407del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.*212_*216del	ENSP00000507912.1:n.*212_*216del
ENST00000683962.1:c.*2657_*2661del	ENSP00000506854.1:n.*2657_*2661del
ENST00000311895.8:c.*212_*216del MANE Select	ENSP00000310520.7:n.*212_*216del
ENST00000311895.7:c.*212_*216del	ENSP00000310520.7:n.*212_*216del
NM_005236.2:c.*212_*216del , LRG_463t1:c.*212_*216del	NP_005227.1:n.*212_*216del
XM_011522424.1:c.*212_*216del	XP_011520726.1:n.*212_*216del
XM_011522425.1:c.*212_*216del	XP_011520727.1:n.*212_*216del
XM_011522426.1:c.*212_*216del	XP_011520728.1:n.*212_*216del
XM_011522427.1:c.*212_*216del	XP_011520729.1:n.*212_*216del
XR_932805.1:n.3073+49_3073+53del
XM_011522424.3:c.*212_*216del	XP_011520726.1:n.*212_*216del
XM_017023043.2:c.*212_*216del	XP_016878532.1:n.*212_*216del
NM_005236.3:c.*212_*216del MANE Select	NP_005227.1:n.*212_*216del