Canonical Allele Identifier: CA2631831576

Gene: ERCC4

Linked Data

• gnomAD v4: 16-13948572-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948572G>A , CM000678.2:g.13948572G>A	GRCh38
NC_000016.9:g.14042429G>A , CM000678.1:g.14042429G>A	GRCh37
NC_000016.8:g.13949930G>A	NCBI36
NG_011442.1:g.33416G>A , LRG_463:g.33416G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.*225G>A	ENSP00000507912.1:n.*225G>A
ENST00000683962.1:c.*2670G>A	ENSP00000506854.1:n.*2670G>A
ENST00000311895.8:c.*225G>A MANE Select	ENSP00000310520.7:n.*225G>A
ENST00000311895.7:c.*225G>A	ENSP00000310520.7:n.*225G>A
NM_005236.2:c.*225G>A , LRG_463t1:c.*225G>A	NP_005227.1:n.*225G>A
XM_011522424.1:c.*225G>A	XP_011520726.1:n.*225G>A
XM_011522425.1:c.*225G>A	XP_011520727.1:n.*225G>A
XM_011522426.1:c.*225G>A	XP_011520728.1:n.*225G>A
XM_011522427.1:c.*225G>A	XP_011520729.1:n.*225G>A
XR_932805.1:n.3073+62G>A
XM_011522424.3:c.*225G>A	XP_011520726.1:n.*225G>A
XM_017023043.2:c.*225G>A	XP_016878532.1:n.*225G>A
NM_005236.3:c.*225G>A MANE Select	NP_005227.1:n.*225G>A