Canonical Allele Identifier: CA2209082934
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948239A= , CM000678.2:g.13948239A= GRCh38
NC_000016.9:g.14042096A= , CM000678.1:g.14042096A= GRCh37
NC_000016.8:g.13949597A= NCBI36
NG_011442.1:g.33083A= , LRG_463:g.33083A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2781A= ENSP00000507912.1:p.Gln927=
ENST00000683962.1:c.*2337A= ENSP00000506854.1:n.*2337A=
ENST00000311895.8:c.2643A= MANE Select ENSP00000310520.7:p.Gln881=
ENST00000311895.7:c.2643A= ENSP00000310520.7:p.Gln881=
ENST00000389138.7:n.1920A=
NM_005236.2:c.2643A= , LRG_463t1:c.2643A= NP_005227.1:p.Gln881=
XM_011522424.1:c.2781A= XP_011520726.1:p.Gln927=
XM_011522425.1:c.2100A= XP_011520727.1:p.Gln700=
XM_011522426.1:c.1854A= XP_011520728.1:p.Gln618=
XM_011522427.1:c.1293A= XP_011520729.1:p.Gln431=
XR_932805.1:n.2802A=
XM_011522424.3:c.2781A= XP_011520726.1:p.Gln927=
XM_017023043.2:c.1854A= XP_016878532.1:p.Gln618=
NM_005236.3:c.2643A= MANE Select NP_005227.1:p.Gln881=