Canonical Allele Identifier: CA2805944176

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947605dup , CM000678.2:g.13947605dup	GRCh38
NC_000016.9:g.14041462dup , CM000678.1:g.14041462dup	GRCh37
NC_000016.8:g.13948963dup	NCBI36
NG_011442.1:g.32449dup , LRG_463:g.32449dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2156-9dup	ENSP00000507912.1:n.2156-9dup
ENST00000683962.1:c.*1712-9dup	ENSP00000506854.1:n.*1712-9dup
ENST00000311895.8:c.2018-9dup MANE Select	ENSP00000310520.7:n.2018-9dup
ENST00000311895.7:c.2018-9dup	ENSP00000310520.7:n.2018-9dup
ENST00000389138.7:n.1295-9dup
ENST00000462862.1:c.331-9dup	ENSP00000461322.1:n.331-9dup
NM_005236.2:c.2018-9dup , LRG_463t1:c.2018-9dup	NP_005227.1:n.2018-9dup
XM_011522424.1:c.2156-9dup	XP_011520726.1:n.2156-9dup
XM_011522425.1:c.1475-9dup	XP_011520727.1:n.1475-9dup
XM_011522426.1:c.1229-9dup	XP_011520728.1:n.1229-9dup
XM_011522427.1:c.668-9dup	XP_011520729.1:n.668-9dup
XR_932805.1:n.2177-9dup
XM_011522424.3:c.2156-9dup	XP_011520726.1:n.2156-9dup
XM_017023043.2:c.1229-9dup	XP_016878532.1:n.1229-9dup
NM_005236.3:c.2018-9dup MANE Select	NP_005227.1:n.2018-9dup