Canonical Allele Identifier: CA493444398

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14038655A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13944798A>T , CM000678.2:g.13944798A>T	GRCh38
NC_000016.9:g.14038655A>T , CM000678.1:g.14038655A>T	GRCh37
NC_000016.8:g.13946156A>T	NCBI36
NG_011442.1:g.29642A>T , LRG_463:g.29642A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2118A>T	ENSP00000507912.1:p.Thr706=
ENST00000683962.1:c.*1674A>T	ENSP00000506854.1:n.*1674A>T
ENST00000311895.8:c.1980A>T MANE Select	ENSP00000310520.7:p.Thr660=
ENST00000311895.7:c.1980A>T	ENSP00000310520.7:p.Thr660=
ENST00000389138.7:n.1257A>T
ENST00000462862.1:c.293A>T	ENSP00000461322.1:n.293A>T
NM_005236.2:c.1980A>T , LRG_463t1:c.1980A>T	NP_005227.1:p.Thr660=
XM_011522424.1:c.2118A>T	XP_011520726.1:p.Thr706=
XM_011522425.1:c.1437A>T	XP_011520727.1:p.Thr479=
XM_011522426.1:c.1191A>T	XP_011520728.1:p.Thr397=
XM_011522427.1:c.630A>T	XP_011520729.1:p.Thr210=
XR_932805.1:n.2139A>T
XM_011522424.3:c.2118A>T	XP_011520726.1:p.Thr706=
XM_017023043.2:c.1191A>T	XP_016878532.1:p.Thr397=
NM_005236.3:c.1980A>T MANE Select	NP_005227.1:p.Thr660=