Canonical Allele Identifier: CA2631831502

Gene: ERCC4

Linked Data

• gnomAD v4: 16-13948502-ACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948505_13948506del , CM000678.2:g.13948505_13948506del	GRCh38
NC_000016.9:g.14042362_14042363del , CM000678.1:g.14042362_14042363del	GRCh37
NC_000016.8:g.13949863_13949864del	NCBI36
NG_011442.1:g.33349_33350del , LRG_463:g.33349_33350del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.*158_*159del	ENSP00000507912.1:n.*158_*159del
ENST00000683962.1:c.*2603_*2604del	ENSP00000506854.1:n.*2603_*2604del
ENST00000311895.8:c.*158_*159del MANE Select	ENSP00000310520.7:n.*158_*159del
ENST00000311895.7:c.*158_*159del	ENSP00000310520.7:n.*158_*159del
NM_005236.2:c.*158_*159del , LRG_463t1:c.*158_*159del	NP_005227.1:n.*158_*159del
XM_011522424.1:c.*158_*159del	XP_011520726.1:n.*158_*159del
XM_011522425.1:c.*158_*159del	XP_011520727.1:n.*158_*159del
XM_011522426.1:c.*158_*159del	XP_011520728.1:n.*158_*159del
XM_011522427.1:c.*158_*159del	XP_011520729.1:n.*158_*159del
XR_932805.1:n.3068_3069del
XM_011522424.3:c.*158_*159del	XP_011520726.1:n.*158_*159del
XM_017023043.2:c.*158_*159del	XP_016878532.1:n.*158_*159del
NM_005236.3:c.*158_*159del MANE Select	NP_005227.1:n.*158_*159del