Canonical Allele Identifier: CA394823852
Gene: ERCC4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948040A>G , CM000678.2:g.13948040A>G GRCh38
NC_000016.9:g.14041897A>G , CM000678.1:g.14041897A>G GRCh37
NC_000016.8:g.13949398A>G NCBI36
NG_011442.1:g.32884A>G , LRG_463:g.32884A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682617.1:c.2582A>G ENSP00000507912.1:p.Glu861Gly
ENST00000683962.1:c.*2138A>G ENSP00000506854.1:n.*2138A>G
ENST00000311895.8:c.2444A>G MANE Select ENSP00000310520.7:p.Glu815Gly
ENST00000311895.7:c.2444A>G ENSP00000310520.7:p.Glu815Gly
ENST00000389138.7:n.1721A>G
NM_005236.2:c.2444A>G , LRG_463t1:c.2444A>G NP_005227.1:p.Glu815Gly
XM_011522424.1:c.2582A>G XP_011520726.1:p.Glu861Gly
XM_011522425.1:c.1901A>G XP_011520727.1:p.Glu634Gly
XM_011522426.1:c.1655A>G XP_011520728.1:p.Glu552Gly
XM_011522427.1:c.1094A>G XP_011520729.1:p.Glu365Gly
XR_932805.1:n.2603A>G
XM_011522424.3:c.2582A>G XP_011520726.1:p.Glu861Gly
XM_017023043.2:c.1655A>G XP_016878532.1:p.Glu552Gly
NM_005236.3:c.2444A>G MANE Select NP_005227.1:p.Glu815Gly