Canonical Allele Identifier: CA2631831439

Gene: ERCC4

Linked Data

• gnomAD v4: 16-13948400-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948400C>A , CM000678.2:g.13948400C>A	GRCh38
NC_000016.9:g.14042257C>A , CM000678.1:g.14042257C>A	GRCh37
NC_000016.8:g.13949758C>A	NCBI36
NG_011442.1:g.33244C>A , LRG_463:g.33244C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.*53C>A	ENSP00000507912.1:n.*53C>A
ENST00000683962.1:c.*2498C>A	ENSP00000506854.1:n.*2498C>A
ENST00000311895.8:c.*53C>A MANE Select	ENSP00000310520.7:n.*53C>A
ENST00000311895.7:c.*53C>A	ENSP00000310520.7:n.*53C>A
ENST00000389138.7:n.2081C>A
NM_005236.2:c.*53C>A , LRG_463t1:c.*53C>A	NP_005227.1:n.*53C>A
XM_011522424.1:c.*53C>A	XP_011520726.1:n.*53C>A
XM_011522425.1:c.*53C>A	XP_011520727.1:n.*53C>A
XM_011522426.1:c.*53C>A	XP_011520728.1:n.*53C>A
XM_011522427.1:c.*53C>A	XP_011520729.1:n.*53C>A
XR_932805.1:n.2963C>A
XM_011522424.3:c.*53C>A	XP_011520726.1:n.*53C>A
XM_017023043.2:c.*53C>A	XP_016878532.1:n.*53C>A
NM_005236.3:c.*53C>A MANE Select	NP_005227.1:n.*53C>A