Canonical Allele Identifier: CA394812791

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14029580T>G (hg19) ; chr16:g.13935723T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935723T>G , CM000678.2:g.13935723T>G	GRCh38
NC_000016.9:g.14029580T>G , CM000678.1:g.14029580T>G	GRCh37
NC_000016.8:g.13937081T>G	NCBI36
NG_011442.1:g.20567T>G , LRG_463:g.20567T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1869T>G
ENST00000682617.1:c.1929T>G	ENSP00000507912.1:p.Ser643Arg
ENST00000682826.1:c.*1105T>G	ENSP00000507274.1:n.*1105T>G
ENST00000682909.1:n.3831T>G
ENST00000683277.1:n.3436T>G
ENST00000683407.1:n.1799T>G
ENST00000683962.1:c.*1485T>G	ENSP00000506854.1:n.*1485T>G
ENST00000311895.8:c.1791T>G MANE Select	ENSP00000310520.7:p.Ser597Arg
ENST00000311895.7:c.1791T>G	ENSP00000310520.7:p.Ser597Arg
ENST00000389138.7:n.1068T>G
NM_005236.2:c.1791T>G , LRG_463t1:c.1791T>G	NP_005227.1:p.Ser597Arg
XM_011522424.1:c.1929T>G	XP_011520726.1:p.Ser643Arg
XM_011522425.1:c.1248T>G	XP_011520727.1:p.Ser416Arg
XM_011522426.1:c.1002T>G	XP_011520728.1:p.Ser334Arg
XM_011522427.1:c.441T>G	XP_011520729.1:p.Ser147Arg
XR_932805.1:n.1950T>G
XM_011522424.3:c.1929T>G	XP_011520726.1:p.Ser643Arg
XM_017023043.2:c.1002T>G	XP_016878532.1:p.Ser334Arg
NM_005236.3:c.1791T>G MANE Select	NP_005227.1:p.Ser597Arg