Canonical Allele Identifier: CA394818009

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14038659T>A (hg19) ; chr16:g.13944802T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13944802T>A , CM000678.2:g.13944802T>A	GRCh38
NC_000016.9:g.14038659T>A , CM000678.1:g.14038659T>A	GRCh37
NC_000016.8:g.13946160T>A	NCBI36
NG_011442.1:g.29646T>A , LRG_463:g.29646T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2122T>A	ENSP00000507912.1:p.Ser708Thr
ENST00000683962.1:c.*1678T>A	ENSP00000506854.1:n.*1678T>A
ENST00000311895.8:c.1984T>A MANE Select	ENSP00000310520.7:p.Ser662Thr
ENST00000311895.7:c.1984T>A	ENSP00000310520.7:p.Ser662Thr
ENST00000389138.7:n.1261T>A
ENST00000462862.1:c.297T>A	ENSP00000461322.1:n.297T>A
NM_005236.2:c.1984T>A , LRG_463t1:c.1984T>A	NP_005227.1:p.Ser662Thr
XM_011522424.1:c.2122T>A	XP_011520726.1:p.Ser708Thr
XM_011522425.1:c.1441T>A	XP_011520727.1:p.Ser481Thr
XM_011522426.1:c.1195T>A	XP_011520728.1:p.Ser399Thr
XM_011522427.1:c.634T>A	XP_011520729.1:p.Ser212Thr
XR_932805.1:n.2143T>A
XM_011522424.3:c.2122T>A	XP_011520726.1:p.Ser708Thr
XM_017023043.2:c.1195T>A	XP_016878532.1:p.Ser399Thr
NM_005236.3:c.1984T>A MANE Select	NP_005227.1:p.Ser662Thr