Canonical Allele Identifier: CA2209082925
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948220A= , CM000678.2:g.13948220A= GRCh38
NC_000016.9:g.14042077A= , CM000678.1:g.14042077A= GRCh37
NC_000016.8:g.13949578A= NCBI36
NG_011442.1:g.33064A= , LRG_463:g.33064A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2762A= ENSP00000507912.1:p.Glu921=
ENST00000683962.1:c.*2318A= ENSP00000506854.1:n.*2318A=
ENST00000311895.8:c.2624A= MANE Select ENSP00000310520.7:p.Glu875=
ENST00000311895.7:c.2624A= ENSP00000310520.7:p.Glu875=
ENST00000389138.7:n.1901A=
NM_005236.2:c.2624A= , LRG_463t1:c.2624A= NP_005227.1:p.Glu875=
XM_011522424.1:c.2762A= XP_011520726.1:p.Glu921=
XM_011522425.1:c.2081A= XP_011520727.1:p.Glu694=
XM_011522426.1:c.1835A= XP_011520728.1:p.Glu612=
XM_011522427.1:c.1274A= XP_011520729.1:p.Glu425=
XR_932805.1:n.2783A=
XM_011522424.3:c.2762A= XP_011520726.1:p.Glu921=
XM_017023043.2:c.1835A= XP_016878532.1:p.Glu612=
NM_005236.3:c.2624A= MANE Select NP_005227.1:p.Glu875=