Canonical Allele Identifier: CA394822277

Gene: ERCC4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947762G>A , CM000678.2:g.13947762G>A	GRCh38
NC_000016.9:g.14041619G>A , CM000678.1:g.14041619G>A	GRCh37
NC_000016.8:g.13949120G>A	NCBI36
NG_011442.1:g.32606G>A , LRG_463:g.32606G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2304G>A	ENSP00000507912.1:p.Met768Ile
ENST00000683962.1:c.*1860G>A	ENSP00000506854.1:n.*1860G>A
ENST00000311895.8:c.2166G>A MANE Select	ENSP00000310520.7:p.Met722Ile
ENST00000311895.7:c.2166G>A	ENSP00000310520.7:p.Met722Ile
ENST00000389138.7:n.1443G>A
ENST00000462862.1:c.479G>A	ENSP00000461322.1:n.479G>A
NM_005236.2:c.2166G>A , LRG_463t1:c.2166G>A	NP_005227.1:p.Met722Ile
XM_011522424.1:c.2304G>A	XP_011520726.1:p.Met768Ile
XM_011522425.1:c.1623G>A	XP_011520727.1:p.Met541Ile
XM_011522426.1:c.1377G>A	XP_011520728.1:p.Met459Ile
XM_011522427.1:c.816G>A	XP_011520729.1:p.Met272Ile
XR_932805.1:n.2325G>A
XM_011522424.3:c.2304G>A	XP_011520726.1:p.Met768Ile
XM_017023043.2:c.1377G>A	XP_016878532.1:p.Met459Ile
NM_005236.3:c.2166G>A MANE Select	NP_005227.1:p.Met722Ile