Canonical Allele Identifier: CA2209082890
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948159A= , CM000678.2:g.13948159A= GRCh38
NC_000016.9:g.14042016A= , CM000678.1:g.14042016A= GRCh37
NC_000016.8:g.13949517A= NCBI36
NG_011442.1:g.33003A= , LRG_463:g.33003A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682617.1:c.2701A= ENSP00000507912.1:p.Met901=
ENST00000683962.1:c.*2257A= ENSP00000506854.1:n.*2257A=
ENST00000311895.8:c.2563A= MANE Select ENSP00000310520.7:p.Met855=
ENST00000311895.7:c.2563A= ENSP00000310520.7:p.Met855=
ENST00000389138.7:n.1840A=
NM_005236.2:c.2563A= , LRG_463t1:c.2563A= NP_005227.1:p.Met855=
XM_011522424.1:c.2701A= XP_011520726.1:p.Met901=
XM_011522425.1:c.2020A= XP_011520727.1:p.Met674=
XM_011522426.1:c.1774A= XP_011520728.1:p.Met592=
XM_011522427.1:c.1213A= XP_011520729.1:p.Met405=
XR_932805.1:n.2722A=
XM_011522424.3:c.2701A= XP_011520726.1:p.Met901=
XM_017023043.2:c.1774A= XP_016878532.1:p.Met592=
NM_005236.3:c.2563A= MANE Select NP_005227.1:p.Met855=