Canonical Allele Identifier: CA493689807

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14041718C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947861C>G , CM000678.2:g.13947861C>G	GRCh38
NC_000016.9:g.14041718C>G , CM000678.1:g.14041718C>G	GRCh37
NC_000016.8:g.13949219C>G	NCBI36
NG_011442.1:g.32705C>G , LRG_463:g.32705C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2403C>G	ENSP00000507912.1:p.Pro801=
ENST00000683962.1:c.*1959C>G	ENSP00000506854.1:n.*1959C>G
ENST00000311895.8:c.2265C>G MANE Select	ENSP00000310520.7:p.Pro755=
ENST00000311895.7:c.2265C>G	ENSP00000310520.7:p.Pro755=
ENST00000389138.7:n.1542C>G
ENST00000462862.1:c.578C>G	ENSP00000461322.1:n.578C>G
NM_005236.2:c.2265C>G , LRG_463t1:c.2265C>G	NP_005227.1:p.Pro755=
XM_011522424.1:c.2403C>G	XP_011520726.1:p.Pro801=
XM_011522425.1:c.1722C>G	XP_011520727.1:p.Pro574=
XM_011522426.1:c.1476C>G	XP_011520728.1:p.Pro492=
XM_011522427.1:c.915C>G	XP_011520729.1:p.Pro305=
XR_932805.1:n.2424C>G
XM_011522424.3:c.2403C>G	XP_011520726.1:p.Pro801=
XM_017023043.2:c.1476C>G	XP_016878532.1:p.Pro492=
NM_005236.3:c.2265C>G MANE Select	NP_005227.1:p.Pro755=