Canonical Allele Identifier: CA394812223

Gene: ERCC4

Linked Data

• dbSNP Id: rs549865610
• MyVariant Identifiers: chr16:g.14029444C>A (hg19) ; chr16:g.13935587C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935587C>A , CM000678.2:g.13935587C>A	GRCh38
NC_000016.9:g.14029444C>A , CM000678.1:g.14029444C>A	GRCh37
NC_000016.8:g.13936945C>A	NCBI36
NG_011442.1:g.20431C>A , LRG_463:g.20431C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1733C>A
ENST00000682617.1:c.1793C>A	ENSP00000507912.1:p.Thr598Asn
ENST00000682826.1:c.*969C>A	ENSP00000507274.1:n.*969C>A
ENST00000682909.1:n.3695C>A
ENST00000683277.1:n.3300C>A
ENST00000683407.1:n.1663C>A
ENST00000683962.1:c.*1349C>A	ENSP00000506854.1:n.*1349C>A
ENST00000311895.8:c.1655C>A MANE Select	ENSP00000310520.7:p.Thr552Asn
ENST00000311895.7:c.1655C>A	ENSP00000310520.7:p.Thr552Asn
ENST00000389138.7:n.932C>A
NM_005236.2:c.1655C>A , LRG_463t1:c.1655C>A	NP_005227.1:p.Thr552Asn
XM_011522424.1:c.1793C>A	XP_011520726.1:p.Thr598Asn
XM_011522425.1:c.1112C>A	XP_011520727.1:p.Thr371Asn
XM_011522426.1:c.866C>A	XP_011520728.1:p.Thr289Asn
XM_011522427.1:c.305C>A	XP_011520729.1:p.Thr102Asn
XR_932805.1:n.1814C>A
XM_011522424.3:c.1793C>A	XP_011520726.1:p.Thr598Asn
XM_017023043.2:c.866C>A	XP_016878532.1:p.Thr289Asn
NM_005236.3:c.1655C>A MANE Select	NP_005227.1:p.Thr552Asn