Canonical Allele Identifier: CA394823968

Gene: ERCC4

Linked Data

• gnomAD v4: 16-13948060-C-G
• MyVariant Identifiers: chr16:g.14041917C>G (hg19) ; chr16:g.13948060C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948060C>G , CM000678.2:g.13948060C>G	GRCh38
NC_000016.9:g.14041917C>G , CM000678.1:g.14041917C>G	GRCh37
NC_000016.8:g.13949418C>G	NCBI36
NG_011442.1:g.32904C>G , LRG_463:g.32904C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2602C>G	ENSP00000507912.1:p.Gln868Glu
ENST00000683962.1:c.*2158C>G	ENSP00000506854.1:n.*2158C>G
ENST00000311895.8:c.2464C>G MANE Select	ENSP00000310520.7:p.Gln822Glu
ENST00000311895.7:c.2464C>G	ENSP00000310520.7:p.Gln822Glu
ENST00000389138.7:n.1741C>G
NM_005236.2:c.2464C>G , LRG_463t1:c.2464C>G	NP_005227.1:p.Gln822Glu
XM_011522424.1:c.2602C>G	XP_011520726.1:p.Gln868Glu
XM_011522425.1:c.1921C>G	XP_011520727.1:p.Gln641Glu
XM_011522426.1:c.1675C>G	XP_011520728.1:p.Gln559Glu
XM_011522427.1:c.1114C>G	XP_011520729.1:p.Gln372Glu
XR_932805.1:n.2623C>G
XM_011522424.3:c.2602C>G	XP_011520726.1:p.Gln868Glu
XM_017023043.2:c.1675C>G	XP_016878532.1:p.Gln559Glu
NM_005236.3:c.2464C>G MANE Select	NP_005227.1:p.Gln822Glu