Canonical Allele Identifier: CA493689898

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14029460T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935603T>G , CM000678.2:g.13935603T>G	GRCh38
NC_000016.9:g.14029460T>G , CM000678.1:g.14029460T>G	GRCh37
NC_000016.8:g.13936961T>G	NCBI36
NG_011442.1:g.20447T>G , LRG_463:g.20447T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1749T>G
ENST00000682617.1:c.1809T>G	ENSP00000507912.1:p.Leu603=
ENST00000682826.1:c.*985T>G	ENSP00000507274.1:n.*985T>G
ENST00000682909.1:n.3711T>G
ENST00000683277.1:n.3316T>G
ENST00000683407.1:n.1679T>G
ENST00000683962.1:c.*1365T>G	ENSP00000506854.1:n.*1365T>G
ENST00000311895.8:c.1671T>G MANE Select	ENSP00000310520.7:p.Leu557=
ENST00000311895.7:c.1671T>G	ENSP00000310520.7:p.Leu557=
ENST00000389138.7:n.948T>G
NM_005236.2:c.1671T>G , LRG_463t1:c.1671T>G	NP_005227.1:p.Leu557=
XM_011522424.1:c.1809T>G	XP_011520726.1:p.Leu603=
XM_011522425.1:c.1128T>G	XP_011520727.1:p.Leu376=
XM_011522426.1:c.882T>G	XP_011520728.1:p.Leu294=
XM_011522427.1:c.321T>G	XP_011520729.1:p.Leu107=
XR_932805.1:n.1830T>G
XM_011522424.3:c.1809T>G	XP_011520726.1:p.Leu603=
XM_017023043.2:c.882T>G	XP_016878532.1:p.Leu294=
NM_005236.3:c.1671T>G MANE Select	NP_005227.1:p.Leu557=