Canonical Allele Identifier: CA2209081410
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13944745C= , CM000678.2:g.13944745C= GRCh38
NC_000016.9:g.14038602C= , CM000678.1:g.14038602C= GRCh37
NC_000016.8:g.13946103C= NCBI36
NG_011442.1:g.29589C= , LRG_463:g.29589C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682617.1:c.2065C= ENSP00000507912.1:p.Pro689=
ENST00000683962.1:c.*1621C= ENSP00000506854.1:n.*1621C=
ENST00000311895.8:c.1927C= MANE Select ENSP00000310520.7:p.Pro643=
ENST00000311895.7:c.1927C= ENSP00000310520.7:p.Pro643=
ENST00000389138.7:n.1204C=
ENST00000462862.1:c.240C= ENSP00000461322.1:n.240C=
NM_005236.2:c.1927C= , LRG_463t1:c.1927C= NP_005227.1:p.Pro643=
XM_011522424.1:c.2065C= XP_011520726.1:p.Pro689=
XM_011522425.1:c.1384C= XP_011520727.1:p.Pro462=
XM_011522426.1:c.1138C= XP_011520728.1:p.Pro380=
XM_011522427.1:c.577C= XP_011520729.1:p.Pro193=
XR_932805.1:n.2086C=
XM_011522424.3:c.2065C= XP_011520726.1:p.Pro689=
XM_017023043.2:c.1138C= XP_016878532.1:p.Pro380=
NM_005236.3:c.1927C= MANE Select NP_005227.1:p.Pro643=