Canonical Allele Identifier: CA2209082874
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948131T= , CM000678.2:g.13948131T= GRCh38
NC_000016.9:g.14041988T= , CM000678.1:g.14041988T= GRCh37
NC_000016.8:g.13949489T= NCBI36
NG_011442.1:g.32975T= , LRG_463:g.32975T=

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2673T= ENSP00000507912.1:p.Asn891=
ENST00000683962.1:c.*2229T= ENSP00000506854.1:n.*2229T=
ENST00000311895.8:c.2535T= MANE Select ENSP00000310520.7:p.Asn845=
ENST00000311895.7:c.2535T= ENSP00000310520.7:p.Asn845=
ENST00000389138.7:n.1812T=
NM_005236.2:c.2535T= , LRG_463t1:c.2535T= NP_005227.1:p.Asn845=
XM_011522424.1:c.2673T= XP_011520726.1:p.Asn891=
XM_011522425.1:c.1992T= XP_011520727.1:p.Asn664=
XM_011522426.1:c.1746T= XP_011520728.1:p.Asn582=
XM_011522427.1:c.1185T= XP_011520729.1:p.Asn395=
XR_932805.1:n.2694T=
XM_011522424.3:c.2673T= XP_011520726.1:p.Asn891=
XM_017023043.2:c.1746T= XP_016878532.1:p.Asn582=
NM_005236.3:c.2535T= MANE Select NP_005227.1:p.Asn845=