Canonical Allele Identifier: CA394822389

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947783C>G , CM000678.2:g.13947783C>G	GRCh38
NC_000016.9:g.14041640C>G , CM000678.1:g.14041640C>G	GRCh37
NC_000016.8:g.13949141C>G	NCBI36
NG_011442.1:g.32627C>G , LRG_463:g.32627C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_005236.3:c.2187C>G MANE Select	NP_005227.1:p.Ile729Met
ENST00000311895.8:c.2187C>G MANE Select	ENSP00000310520.7:p.Ile729Met
NM_005236.2:c.2187C>G , LRG_463t1:c.2187C>G	NP_005227.1:p.Ile729Met
ENST00000311895.7:c.2187C>G	ENSP00000310520.7:p.Ile729Met
ENST00000389138.7:n.1464C>G
ENST00000462862.1:c.500C>G	ENSP00000461322.1:n.500C>G
ENST00000682617.1:c.2325C>G	ENSP00000507912.1:p.Ile775Met
ENST00000683962.1:c.*1881C>G	ENSP00000506854.1:n.*1881C>G
XM_011522424.1:c.2325C>G	XP_011520726.1:p.Ile775Met
XM_011522424.3:c.2325C>G	XP_011520726.1:p.Ile775Met
XM_011522425.1:c.1644C>G	XP_011520727.1:p.Ile548Met
XM_011522426.1:c.1398C>G	XP_011520728.1:p.Ile466Met
XM_011522427.1:c.837C>G	XP_011520729.1:p.Ile279Met
XM_017023043.2:c.1398C>G	XP_016878532.1:p.Ile466Met
XR_932805.1:n.2346C>G