Canonical Allele Identifier: CA394823668

Gene: ERCC4

Linked Data

• dbSNP Id: rs1417008993
• gnomAD v2: 16-14041878-A-G
• gnomAD v4: 16-13948021-A-G
• MyVariant Identifiers: chr16:g.14041878A>G (hg19) ; chr16:g.13948021A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948021A>G , CM000678.2:g.13948021A>G	GRCh38
NC_000016.9:g.14041878A>G , CM000678.1:g.14041878A>G	GRCh37
NC_000016.8:g.13949379A>G	NCBI36
NG_011442.1:g.32865A>G , LRG_463:g.32865A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2563A>G	ENSP00000507912.1:p.Thr855Ala
ENST00000683962.1:c.*2119A>G	ENSP00000506854.1:n.*2119A>G
ENST00000311895.8:c.2425A>G MANE Select	ENSP00000310520.7:p.Thr809Ala
ENST00000311895.7:c.2425A>G	ENSP00000310520.7:p.Thr809Ala
ENST00000389138.7:n.1702A>G
NM_005236.2:c.2425A>G , LRG_463t1:c.2425A>G	NP_005227.1:p.Thr809Ala
XM_011522424.1:c.2563A>G	XP_011520726.1:p.Thr855Ala
XM_011522425.1:c.1882A>G	XP_011520727.1:p.Thr628Ala
XM_011522426.1:c.1636A>G	XP_011520728.1:p.Thr546Ala
XM_011522427.1:c.1075A>G	XP_011520729.1:p.Thr359Ala
XR_932805.1:n.2584A>G
XM_011522424.3:c.2563A>G	XP_011520726.1:p.Thr855Ala
XM_017023043.2:c.1636A>G	XP_016878532.1:p.Thr546Ala
NM_005236.3:c.2425A>G MANE Select	NP_005227.1:p.Thr809Ala