Canonical Allele Identifier: CA493689805

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14041715T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947858T>C , CM000678.2:g.13947858T>C	GRCh38
NC_000016.9:g.14041715T>C , CM000678.1:g.14041715T>C	GRCh37
NC_000016.8:g.13949216T>C	NCBI36
NG_011442.1:g.32702T>C , LRG_463:g.32702T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2400T>C	ENSP00000507912.1:p.Arg800=
ENST00000683962.1:c.*1956T>C	ENSP00000506854.1:n.*1956T>C
ENST00000311895.8:c.2262T>C MANE Select	ENSP00000310520.7:p.Arg754=
ENST00000311895.7:c.2262T>C	ENSP00000310520.7:p.Arg754=
ENST00000389138.7:n.1539T>C
ENST00000462862.1:c.575T>C	ENSP00000461322.1:n.575T>C
NM_005236.2:c.2262T>C , LRG_463t1:c.2262T>C	NP_005227.1:p.Arg754=
XM_011522424.1:c.2400T>C	XP_011520726.1:p.Arg800=
XM_011522425.1:c.1719T>C	XP_011520727.1:p.Arg573=
XM_011522426.1:c.1473T>C	XP_011520728.1:p.Arg491=
XM_011522427.1:c.912T>C	XP_011520729.1:p.Arg304=
XR_932805.1:n.2421T>C
XM_011522424.3:c.2400T>C	XP_011520726.1:p.Arg800=
XM_017023043.2:c.1473T>C	XP_016878532.1:p.Arg491=
NM_005236.3:c.2262T>C MANE Select	NP_005227.1:p.Arg754=