Canonical Allele Identifier: CA493444434

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14041484G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947627G>A , CM000678.2:g.13947627G>A	GRCh38
NC_000016.9:g.14041484G>A , CM000678.1:g.14041484G>A	GRCh37
NC_000016.8:g.13948985G>A	NCBI36
NG_011442.1:g.32471G>A , LRG_463:g.32471G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2169G>A	ENSP00000507912.1:p.Gln723=
ENST00000683962.1:c.*1725G>A	ENSP00000506854.1:n.*1725G>A
ENST00000311895.8:c.2031G>A MANE Select	ENSP00000310520.7:p.Gln677=
ENST00000311895.7:c.2031G>A	ENSP00000310520.7:p.Gln677=
ENST00000389138.7:n.1308G>A
ENST00000462862.1:c.344G>A	ENSP00000461322.1:n.344G>A
NM_005236.2:c.2031G>A , LRG_463t1:c.2031G>A	NP_005227.1:p.Gln677=
XM_011522424.1:c.2169G>A	XP_011520726.1:p.Gln723=
XM_011522425.1:c.1488G>A	XP_011520727.1:p.Gln496=
XM_011522426.1:c.1242G>A	XP_011520728.1:p.Gln414=
XM_011522427.1:c.681G>A	XP_011520729.1:p.Gln227=
XR_932805.1:n.2190G>A
XM_011522424.3:c.2169G>A	XP_011520726.1:p.Gln723=
XM_017023043.2:c.1242G>A	XP_016878532.1:p.Gln414=
NM_005236.3:c.2031G>A MANE Select	NP_005227.1:p.Gln677=