Canonical Allele Identifier: CA1908749349
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49470329G= , CM000672.2:g.49470329G= GRCh38
NC_000010.10:g.50678375G= , CM000672.1:g.50678375G= GRCh37
NC_000010.9:g.50348381G= NCBI36
NG_009442.1:g.73773C= , LRG_465:g.73773C=

Transcript Alleles

HGVS Amino-acid change
ENST00000355832.10:c.3631C= MANE Select ENSP00000348089.5:p.His1211=
ENST00000679552.1:n.702C=
ENST00000679871.1:n.777C=
ENST00000679974.1:n.680C=
ENST00000681632.1:n.5034C=
ENST00000681659.1:c.3472C= ENSP00000505631.1:p.His1158=
ENST00000355832.9:c.3631C= ENSP00000348089.5:p.His1211=
ENST00000623073.3:c.*1927C= ENSP00000485650.1:n.*1927C=
ENST00000623115.3:c.1741C= ENSP00000485321.1:p.His581=
ENST00000624341.3:c.1463C=
NM_000124.3:c.3631C= NP_000115.1:p.His1211=
XR_945953.1:n.243-1236G=
NM_001346440.1:c.3631C= NP_001333369.1:p.His1211=
NM_000124.4:c.3631C= MANE Select NP_000115.1:p.His1211=
NM_001346440.2:c.3631C= NP_001333369.1:p.His1211=