Canonical Allele Identifier: CA1908749345
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49470324G= , CM000672.2:g.49470324G= GRCh38
NC_000010.10:g.50678370G= , CM000672.1:g.50678370G= GRCh37
NC_000010.9:g.50348376G= NCBI36
NG_009442.1:g.73778C= , LRG_465:g.73778C=

Transcript Alleles

HGVS Amino-acid change
ENST00000355832.10:c.3636C= MANE Select ENSP00000348089.5:p.Cys1212=
ENST00000679552.1:n.707C=
ENST00000679871.1:n.782C=
ENST00000679974.1:n.685C=
ENST00000681632.1:n.5039C=
ENST00000681659.1:c.3477C= ENSP00000505631.1:p.Cys1159=
ENST00000355832.9:c.3636C= ENSP00000348089.5:p.Cys1212=
ENST00000623073.3:c.*1932C= ENSP00000485650.1:n.*1932C=
ENST00000623115.3:c.1746C= ENSP00000485321.1:p.Cys582=
ENST00000624341.3:c.1468C=
NM_000124.3:c.3636C= NP_000115.1:p.Cys1212=
XR_945953.1:n.243-1241G=
NM_001346440.1:c.3636C= NP_001333369.1:p.Cys1212=
NM_000124.4:c.3636C= MANE Select NP_000115.1:p.Cys1212=
NM_001346440.2:c.3636C= NP_001333369.1:p.Cys1212=