Canonical Allele Identifier: CA394823214

Gene: ERCC4

Linked Data

• dbSNP Id: rs2032552789
• gnomAD v3: 16-13947962-C-G
• gnomAD v4: 16-13947962-C-G
• MyVariant Identifiers: chr16:g.14041819C>G (hg19) ; chr16:g.13947962C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947962C>G , CM000678.2:g.13947962C>G	GRCh38
NC_000016.9:g.14041819C>G , CM000678.1:g.14041819C>G	GRCh37
NC_000016.8:g.13949320C>G	NCBI36
NG_011442.1:g.32806C>G , LRG_463:g.32806C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2504C>G	ENSP00000507912.1:p.Thr835Ser
ENST00000683962.1:c.*2060C>G	ENSP00000506854.1:n.*2060C>G
ENST00000311895.8:c.2366C>G MANE Select	ENSP00000310520.7:p.Thr789Ser
ENST00000311895.7:c.2366C>G	ENSP00000310520.7:p.Thr789Ser
ENST00000389138.7:n.1643C>G
ENST00000462862.1:c.679C>G	ENSP00000461322.1:n.679C>G
NM_005236.2:c.2366C>G , LRG_463t1:c.2366C>G	NP_005227.1:p.Thr789Ser
XM_011522424.1:c.2504C>G	XP_011520726.1:p.Thr835Ser
XM_011522425.1:c.1823C>G	XP_011520727.1:p.Thr608Ser
XM_011522426.1:c.1577C>G	XP_011520728.1:p.Thr526Ser
XM_011522427.1:c.1016C>G	XP_011520729.1:p.Thr339Ser
XR_932805.1:n.2525C>G
XM_011522424.3:c.2504C>G	XP_011520726.1:p.Thr835Ser
XM_017023043.2:c.1577C>G	XP_016878532.1:p.Thr526Ser
NM_005236.3:c.2366C>G MANE Select	NP_005227.1:p.Thr789Ser