Canonical Allele Identifier: CA394822205

Gene: ERCC4

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947747C>G , CM000678.2:g.13947747C>G	GRCh38
NC_000016.9:g.14041604C>G , CM000678.1:g.14041604C>G	GRCh37
NC_000016.8:g.13949105C>G	NCBI36
NG_011442.1:g.32591C>G , LRG_463:g.32591C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2289C>G	ENSP00000507912.1:p.Ile763Met
ENST00000683962.1:c.*1845C>G	ENSP00000506854.1:n.*1845C>G
ENST00000311895.8:c.2151C>G MANE Select	ENSP00000310520.7:p.Ile717Met
ENST00000311895.7:c.2151C>G	ENSP00000310520.7:p.Ile717Met
ENST00000389138.7:n.1428C>G
ENST00000462862.1:c.464C>G	ENSP00000461322.1:n.464C>G
NM_005236.2:c.2151C>G , LRG_463t1:c.2151C>G	NP_005227.1:p.Ile717Met
XM_011522424.1:c.2289C>G	XP_011520726.1:p.Ile763Met
XM_011522425.1:c.1608C>G	XP_011520727.1:p.Ile536Met
XM_011522426.1:c.1362C>G	XP_011520728.1:p.Ile454Met
XM_011522427.1:c.801C>G	XP_011520729.1:p.Ile267Met
XR_932805.1:n.2310C>G
XM_011522424.3:c.2289C>G	XP_011520726.1:p.Ile763Met
XM_017023043.2:c.1362C>G	XP_016878532.1:p.Ile454Met
NM_005236.3:c.2151C>G MANE Select	NP_005227.1:p.Ile717Met