Canonical Allele Identifier: CA2209083120
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948636A= , CM000678.2:g.13948636A= GRCh38
NC_000016.9:g.14042493A= , CM000678.1:g.14042493A= GRCh37
NC_000016.8:g.13949994A= NCBI36
NG_011442.1:g.33480A= , LRG_463:g.33480A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682617.1:c.*289A= ENSP00000507912.1:n.*289A=
ENST00000683962.1:c.*2734A= ENSP00000506854.1:n.*2734A=
ENST00000311895.8:c.*289A= MANE Select ENSP00000310520.7:n.*289A=
ENST00000311895.7:c.*289A= ENSP00000310520.7:n.*289A=
NM_005236.2:c.*289A= , LRG_463t1:c.*289A= NP_005227.1:n.*289A=
XM_011522424.1:c.*289A= XP_011520726.1:n.*289A=
XM_011522425.1:c.*289A= XP_011520727.1:n.*289A=
XM_011522426.1:c.*289A= XP_011520728.1:n.*289A=
XM_011522427.1:c.*289A= XP_011520729.1:n.*289A=
XR_932805.1:n.3074-77A=
XM_011522424.3:c.*289A= XP_011520726.1:n.*289A=
XM_017023043.2:c.*289A= XP_016878532.1:n.*289A=
NM_005236.3:c.*289A= MANE Select NP_005227.1:n.*289A=