Canonical Allele Identifier: CA2209082835
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948029G= , CM000678.2:g.13948029G= GRCh38
NC_000016.9:g.14041886G= , CM000678.1:g.14041886G= GRCh37
NC_000016.8:g.13949387G= NCBI36
NG_011442.1:g.32873G= , LRG_463:g.32873G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2571G= ENSP00000507912.1:p.Glu857=
ENST00000683962.1:c.*2127G= ENSP00000506854.1:n.*2127G=
ENST00000311895.8:c.2433G= MANE Select ENSP00000310520.7:p.Glu811=
ENST00000311895.7:c.2433G= ENSP00000310520.7:p.Glu811=
ENST00000389138.7:n.1710G=
NM_005236.2:c.2433G= , LRG_463t1:c.2433G= NP_005227.1:p.Glu811=
XM_011522424.1:c.2571G= XP_011520726.1:p.Glu857=
XM_011522425.1:c.1890G= XP_011520727.1:p.Glu630=
XM_011522426.1:c.1644G= XP_011520728.1:p.Glu548=
XM_011522427.1:c.1083G= XP_011520729.1:p.Glu361=
XR_932805.1:n.2592G=
XM_011522424.3:c.2571G= XP_011520726.1:p.Glu857=
XM_017023043.2:c.1644G= XP_016878532.1:p.Glu548=
NM_005236.3:c.2433G= MANE Select NP_005227.1:p.Glu811=