Canonical Allele Identifier: CA2209082831
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948024G= , CM000678.2:g.13948024G= GRCh38
NC_000016.9:g.14041881G= , CM000678.1:g.14041881G= GRCh37
NC_000016.8:g.13949382G= NCBI36
NG_011442.1:g.32868G= , LRG_463:g.32868G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2566G= ENSP00000507912.1:p.Ala856=
ENST00000683962.1:c.*2122G= ENSP00000506854.1:n.*2122G=
ENST00000311895.8:c.2428G= MANE Select ENSP00000310520.7:p.Ala810=
ENST00000311895.7:c.2428G= ENSP00000310520.7:p.Ala810=
ENST00000389138.7:n.1705G=
NM_005236.2:c.2428G= , LRG_463t1:c.2428G= NP_005227.1:p.Ala810=
XM_011522424.1:c.2566G= XP_011520726.1:p.Ala856=
XM_011522425.1:c.1885G= XP_011520727.1:p.Ala629=
XM_011522426.1:c.1639G= XP_011520728.1:p.Ala547=
XM_011522427.1:c.1078G= XP_011520729.1:p.Ala360=
XR_932805.1:n.2587G=
XM_011522424.3:c.2566G= XP_011520726.1:p.Ala856=
XM_017023043.2:c.1639G= XP_016878532.1:p.Ala547=
NM_005236.3:c.2428G= MANE Select NP_005227.1:p.Ala810=