Canonical Allele Identifier: CA493444536

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14042183A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948326A>G , CM000678.2:g.13948326A>G	GRCh38
NC_000016.9:g.14042183A>G , CM000678.1:g.14042183A>G	GRCh37
NC_000016.8:g.13949684A>G	NCBI36
NG_011442.1:g.33170A>G , LRG_463:g.33170A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2868A>G	ENSP00000507912.1:p.Ser956=
ENST00000683962.1:c.*2424A>G	ENSP00000506854.1:n.*2424A>G
ENST00000311895.8:c.2730A>G MANE Select	ENSP00000310520.7:p.Ser910=
ENST00000311895.7:c.2730A>G	ENSP00000310520.7:p.Ser910=
ENST00000389138.7:n.2007A>G
NM_005236.2:c.2730A>G , LRG_463t1:c.2730A>G	NP_005227.1:p.Ser910=
XM_011522424.1:c.2868A>G	XP_011520726.1:p.Ser956=
XM_011522425.1:c.2187A>G	XP_011520727.1:p.Ser729=
XM_011522426.1:c.1941A>G	XP_011520728.1:p.Ser647=
XM_011522427.1:c.1380A>G	XP_011520729.1:p.Ser460=
XR_932805.1:n.2889A>G
XM_011522424.3:c.2868A>G	XP_011520726.1:p.Ser956=
XM_017023043.2:c.1941A>G	XP_016878532.1:p.Ser647=
NM_005236.3:c.2730A>G MANE Select	NP_005227.1:p.Ser910=