Canonical Allele Identifier: CA493690074

Gene: ERCC4

Linked Data

• gnomAD v4: 16-13948050-A-G
• MyVariant Identifiers: chr16:g.14041907A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948050A>G , CM000678.2:g.13948050A>G	GRCh38
NC_000016.9:g.14041907A>G , CM000678.1:g.14041907A>G	GRCh37
NC_000016.8:g.13949408A>G	NCBI36
NG_011442.1:g.32894A>G , LRG_463:g.32894A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2592A>G	ENSP00000507912.1:p.Gln864=
ENST00000683962.1:c.*2148A>G	ENSP00000506854.1:n.*2148A>G
ENST00000311895.8:c.2454A>G MANE Select	ENSP00000310520.7:p.Gln818=
ENST00000311895.7:c.2454A>G	ENSP00000310520.7:p.Gln818=
ENST00000389138.7:n.1731A>G
NM_005236.2:c.2454A>G , LRG_463t1:c.2454A>G	NP_005227.1:p.Gln818=
XM_011522424.1:c.2592A>G	XP_011520726.1:p.Gln864=
XM_011522425.1:c.1911A>G	XP_011520727.1:p.Gln637=
XM_011522426.1:c.1665A>G	XP_011520728.1:p.Gln555=
XM_011522427.1:c.1104A>G	XP_011520729.1:p.Gln368=
XR_932805.1:n.2613A>G
XM_011522424.3:c.2592A>G	XP_011520726.1:p.Gln864=
XM_017023043.2:c.1665A>G	XP_016878532.1:p.Gln555=
NM_005236.3:c.2454A>G MANE Select	NP_005227.1:p.Gln818=