Canonical Allele Identifier: CA394811222

Gene: ERCC4

Linked Data

• dbSNP Id: rs1328914945
• gnomAD v2: 16-14029288-A-G
• gnomAD v3: 16-13935431-A-G
• gnomAD v4: 16-13935431-A-G
• MyVariant Identifiers: chr16:g.14029288A>G (hg19) ; chr16:g.13935431A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935431A>G , CM000678.2:g.13935431A>G	GRCh38
NC_000016.9:g.14029288A>G , CM000678.1:g.14029288A>G	GRCh37
NC_000016.8:g.13936789A>G	NCBI36
NG_011442.1:g.20275A>G , LRG_463:g.20275A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1577A>G
ENST00000682617.1:c.1637A>G	ENSP00000507912.1:p.Lys546Arg
ENST00000682826.1:c.*813A>G	ENSP00000507274.1:n.*813A>G
ENST00000682909.1:n.3539A>G
ENST00000683277.1:n.3144A>G
ENST00000683407.1:n.1507A>G
ENST00000683962.1:c.*1193A>G	ENSP00000506854.1:n.*1193A>G
ENST00000311895.8:c.1499A>G MANE Select	ENSP00000310520.7:p.Lys500Arg
ENST00000311895.7:c.1499A>G	ENSP00000310520.7:p.Lys500Arg
ENST00000389138.7:n.776A>G
NM_005236.2:c.1499A>G , LRG_463t1:c.1499A>G	NP_005227.1:p.Lys500Arg
XM_011522424.1:c.1637A>G	XP_011520726.1:p.Lys546Arg
XM_011522425.1:c.956A>G	XP_011520727.1:p.Lys319Arg
XM_011522426.1:c.710A>G	XP_011520728.1:p.Lys237Arg
XM_011522427.1:c.149A>G	XP_011520729.1:p.Lys50Arg
XR_932805.1:n.1658A>G
XM_011522424.3:c.1637A>G	XP_011520726.1:p.Lys546Arg
XM_017023043.2:c.710A>G	XP_016878532.1:p.Lys237Arg
NM_005236.3:c.1499A>G MANE Select	NP_005227.1:p.Lys500Arg