Canonical Allele Identifier: CA493689762

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14041658T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947801T>G , CM000678.2:g.13947801T>G	GRCh38
NC_000016.9:g.14041658T>G , CM000678.1:g.14041658T>G	GRCh37
NC_000016.8:g.13949159T>G	NCBI36
NG_011442.1:g.32645T>G , LRG_463:g.32645T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2343T>G	ENSP00000507912.1:p.Ser781=
ENST00000683962.1:c.*1899T>G	ENSP00000506854.1:n.*1899T>G
ENST00000311895.8:c.2205T>G MANE Select	ENSP00000310520.7:p.Ser735=
ENST00000311895.7:c.2205T>G	ENSP00000310520.7:p.Ser735=
ENST00000389138.7:n.1482T>G
ENST00000462862.1:c.518T>G	ENSP00000461322.1:n.518T>G
NM_005236.2:c.2205T>G , LRG_463t1:c.2205T>G	NP_005227.1:p.Ser735=
XM_011522424.1:c.2343T>G	XP_011520726.1:p.Ser781=
XM_011522425.1:c.1662T>G	XP_011520727.1:p.Ser554=
XM_011522426.1:c.1416T>G	XP_011520728.1:p.Ser472=
XM_011522427.1:c.855T>G	XP_011520729.1:p.Ser285=
XR_932805.1:n.2364T>G
XM_011522424.3:c.2343T>G	XP_011520726.1:p.Ser781=
XM_017023043.2:c.1416T>G	XP_016878532.1:p.Ser472=
NM_005236.3:c.2205T>G MANE Select	NP_005227.1:p.Ser735=