Canonical Allele Identifier: CA394822865

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14041745C>A (hg19) ; chr16:g.13947888C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947888C>A , CM000678.2:g.13947888C>A	GRCh38
NC_000016.9:g.14041745C>A , CM000678.1:g.14041745C>A	GRCh37
NC_000016.8:g.13949246C>A	NCBI36
NG_011442.1:g.32732C>A , LRG_463:g.32732C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2430C>A	ENSP00000507912.1:p.Ser810Arg
ENST00000683962.1:c.*1986C>A	ENSP00000506854.1:n.*1986C>A
ENST00000311895.8:c.2292C>A MANE Select	ENSP00000310520.7:p.Ser764Arg
ENST00000311895.7:c.2292C>A	ENSP00000310520.7:p.Ser764Arg
ENST00000389138.7:n.1569C>A
ENST00000462862.1:c.605C>A	ENSP00000461322.1:n.605C>A
NM_005236.2:c.2292C>A , LRG_463t1:c.2292C>A	NP_005227.1:p.Ser764Arg
XM_011522424.1:c.2430C>A	XP_011520726.1:p.Ser810Arg
XM_011522425.1:c.1749C>A	XP_011520727.1:p.Ser583Arg
XM_011522426.1:c.1503C>A	XP_011520728.1:p.Ser501Arg
XM_011522427.1:c.942C>A	XP_011520729.1:p.Ser314Arg
XR_932805.1:n.2451C>A
XM_011522424.3:c.2430C>A	XP_011520726.1:p.Ser810Arg
XM_017023043.2:c.1503C>A	XP_016878532.1:p.Ser501Arg
NM_005236.3:c.2292C>A MANE Select	NP_005227.1:p.Ser764Arg