Canonical Allele Identifier: CA493689632

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14041550C>T (hg19)

Genomic Alleles

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

Transcript Alleles

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