Canonical Allele Identifier: CA2209083104
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948603T= , CM000678.2:g.13948603T= GRCh38
NC_000016.9:g.14042460T= , CM000678.1:g.14042460T= GRCh37
NC_000016.8:g.13949961T= NCBI36
NG_011442.1:g.33447T= , LRG_463:g.33447T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682617.1:c.*256T= ENSP00000507912.1:n.*256T=
ENST00000683962.1:c.*2701T= ENSP00000506854.1:n.*2701T=
ENST00000311895.8:c.*256T= MANE Select ENSP00000310520.7:n.*256T=
ENST00000311895.7:c.*256T= ENSP00000310520.7:n.*256T=
NM_005236.2:c.*256T= , LRG_463t1:c.*256T= NP_005227.1:n.*256T=
XM_011522424.1:c.*256T= XP_011520726.1:n.*256T=
XM_011522425.1:c.*256T= XP_011520727.1:n.*256T=
XM_011522426.1:c.*256T= XP_011520728.1:n.*256T=
XM_011522427.1:c.*256T= XP_011520729.1:n.*256T=
XR_932805.1:n.3073+93T=
XM_011522424.3:c.*256T= XP_011520726.1:n.*256T=
XM_017023043.2:c.*256T= XP_016878532.1:n.*256T=
NM_005236.3:c.*256T= MANE Select NP_005227.1:n.*256T=