Canonical Allele Identifier: CA493690001

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14041793C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947936C>A , CM000678.2:g.13947936C>A	GRCh38
NC_000016.9:g.14041793C>A , CM000678.1:g.14041793C>A	GRCh37
NC_000016.8:g.13949294C>A	NCBI36
NG_011442.1:g.32780C>A , LRG_463:g.32780C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2478C>A	ENSP00000507912.1:p.Ser826=
ENST00000683962.1:c.*2034C>A	ENSP00000506854.1:n.*2034C>A
ENST00000311895.8:c.2340C>A MANE Select	ENSP00000310520.7:p.Ser780=
ENST00000311895.7:c.2340C>A	ENSP00000310520.7:p.Ser780=
ENST00000389138.7:n.1617C>A
ENST00000462862.1:c.653C>A	ENSP00000461322.1:n.653C>A
NM_005236.2:c.2340C>A , LRG_463t1:c.2340C>A	NP_005227.1:p.Ser780=
XM_011522424.1:c.2478C>A	XP_011520726.1:p.Ser826=
XM_011522425.1:c.1797C>A	XP_011520727.1:p.Ser599=
XM_011522426.1:c.1551C>A	XP_011520728.1:p.Ser517=
XM_011522427.1:c.990C>A	XP_011520729.1:p.Ser330=
XR_932805.1:n.2499C>A
XM_011522424.3:c.2478C>A	XP_011520726.1:p.Ser826=
XM_017023043.2:c.1551C>A	XP_016878532.1:p.Ser517=
NM_005236.3:c.2340C>A MANE Select	NP_005227.1:p.Ser780=