Canonical Allele Identifier: CA7910676

Gene: ERCC4

Linked Data

• ClinVar Variation Id: 2929491
• ClinVar RCV Id: RCV003784657
• dbSNP Id: rs556423345
• ExAC: 16:14041550 C / A
• gnomAD v2: 16-14041550-C-A
• gnomAD v3: 16-13947693-C-A
• gnomAD v4: 16-13947693-C-A
• MyVariant Identifiers: chr16:g.14041550C>A (hg19) ; chr16:g.13947693C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947693C>A , CM000678.2:g.13947693C>A	GRCh38
NC_000016.9:g.14041550C>A , CM000678.1:g.14041550C>A	GRCh37
NC_000016.8:g.13949051C>A	NCBI36
NG_011442.1:g.32537C>A , LRG_463:g.32537C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2235C>A	ENSP00000507912.1:p.Ile745=
ENST00000683962.1:c.*1791C>A	ENSP00000506854.1:n.*1791C>A
ENST00000311895.8:c.2097C>A MANE Select	ENSP00000310520.7:p.Ile699=
ENST00000311895.7:c.2097C>A	ENSP00000310520.7:p.Ile699=
ENST00000389138.7:n.1374C>A
ENST00000462862.1:c.410C>A	ENSP00000461322.1:n.410C>A
NM_005236.2:c.2097C>A , LRG_463t1:c.2097C>A	NP_005227.1:p.Ile699=
XM_011522424.1:c.2235C>A	XP_011520726.1:p.Ile745=
XM_011522425.1:c.1554C>A	XP_011520727.1:p.Ile518=
XM_011522426.1:c.1308C>A	XP_011520728.1:p.Ile436=
XM_011522427.1:c.747C>A	XP_011520729.1:p.Ile249=
XR_932805.1:n.2256C>A
XM_011522424.3:c.2235C>A	XP_011520726.1:p.Ile745=
XM_017023043.2:c.1308C>A	XP_016878532.1:p.Ile436=
NM_005236.3:c.2097C>A MANE Select	NP_005227.1:p.Ile699=