Canonical Allele Identifier: CA2209083071

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948529_13948530delinsTG , CM000678.2:g.13948529_13948530delinsTG	GRCh38
NC_000016.9:g.14042386_14042387delinsTG , CM000678.1:g.14042386_14042387delinsTG	GRCh37
NC_000016.8:g.13949887_13949888delinsTG	NCBI36
NG_011442.1:g.33373_33374delinsTG , LRG_463:g.33373_33374delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.*182_*183delinsTG	ENSP00000507912.1:n.*182_*183delinsTG
ENST00000683962.1:c.*2627_*2628delinsTG	ENSP00000506854.1:n.*2627_*2628delinsTG
ENST00000311895.8:c.*182_*183delinsTG MANE Select	ENSP00000310520.7:n.*182_*183delinsTG
ENST00000311895.7:c.*182_*183delinsTG	ENSP00000310520.7:n.*182_*183delinsTG
NM_005236.2:c.*182_*183delinsTG , LRG_463t1:c.*182_*183delinsTG	NP_005227.1:n.*182_*183delinsTG
XM_011522424.1:c.*182_*183delinsTG	XP_011520726.1:n.*182_*183delinsTG
XM_011522425.1:c.*182_*183delinsTG	XP_011520727.1:n.*182_*183delinsTG
XM_011522426.1:c.*182_*183delinsTG	XP_011520728.1:n.*182_*183delinsTG
XM_011522427.1:c.*182_*183delinsTG	XP_011520729.1:n.*182_*183delinsTG
XR_932805.1:n.3073+19_3073+20delinsTG
XM_011522424.3:c.*182_*183delinsTG	XP_011520726.1:n.*182_*183delinsTG
XM_017023043.2:c.*182_*183delinsTG	XP_016878532.1:n.*182_*183delinsTG
NM_005236.3:c.*182_*183delinsTG MANE Select	NP_005227.1:n.*182_*183delinsTG