Canonical Allele Identifier: CA394823561

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948005C>G , CM000678.2:g.13948005C>G	GRCh38
NC_000016.9:g.14041862C>G , CM000678.1:g.14041862C>G	GRCh37
NC_000016.8:g.13949363C>G	NCBI36
NG_011442.1:g.32849C>G , LRG_463:g.32849C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_005236.3:c.2409C>G MANE Select	NP_005227.1:p.Cys803Trp
ENST00000311895.8:c.2409C>G MANE Select	ENSP00000310520.7:p.Cys803Trp
NM_005236.2:c.2409C>G , LRG_463t1:c.2409C>G	NP_005227.1:p.Cys803Trp
ENST00000311895.7:c.2409C>G	ENSP00000310520.7:p.Cys803Trp
ENST00000389138.7:n.1686C>G
ENST00000682617.1:c.2547C>G	ENSP00000507912.1:p.Cys849Trp
ENST00000683962.1:c.*2103C>G	ENSP00000506854.1:n.*2103C>G
XM_011522424.1:c.2547C>G	XP_011520726.1:p.Cys849Trp
XM_011522424.3:c.2547C>G	XP_011520726.1:p.Cys849Trp
XM_011522425.1:c.1866C>G	XP_011520727.1:p.Cys622Trp
XM_011522426.1:c.1620C>G	XP_011520728.1:p.Cys540Trp
XM_011522427.1:c.1059C>G	XP_011520729.1:p.Cys353Trp
XM_017023043.2:c.1620C>G	XP_016878532.1:p.Cys540Trp
XR_932805.1:n.2568C>G