Canonical Allele Identifier: CA493444409

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14038670T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13944813T>A , CM000678.2:g.13944813T>A	GRCh38
NC_000016.9:g.14038670T>A , CM000678.1:g.14038670T>A	GRCh37
NC_000016.8:g.13946171T>A	NCBI36
NG_011442.1:g.29657T>A , LRG_463:g.29657T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2133T>A	ENSP00000507912.1:p.Val711=
ENST00000683962.1:c.*1689T>A	ENSP00000506854.1:n.*1689T>A
ENST00000311895.8:c.1995T>A MANE Select	ENSP00000310520.7:p.Val665=
ENST00000311895.7:c.1995T>A	ENSP00000310520.7:p.Val665=
ENST00000389138.7:n.1272T>A
ENST00000462862.1:c.308T>A	ENSP00000461322.1:n.308T>A
NM_005236.2:c.1995T>A , LRG_463t1:c.1995T>A	NP_005227.1:p.Val665=
XM_011522424.1:c.2133T>A	XP_011520726.1:p.Val711=
XM_011522425.1:c.1452T>A	XP_011520727.1:p.Val484=
XM_011522426.1:c.1206T>A	XP_011520728.1:p.Val402=
XM_011522427.1:c.645T>A	XP_011520729.1:p.Val215=
XR_932805.1:n.2154T>A
XM_011522424.3:c.2133T>A	XP_011520726.1:p.Val711=
XM_017023043.2:c.1206T>A	XP_016878532.1:p.Val402=
NM_005236.3:c.1995T>A MANE Select	NP_005227.1:p.Val665=