Canonical Allele Identifier: CA1908760460
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49482809G= , CM000672.2:g.49482809G= GRCh38
NC_000010.10:g.50690855G= , CM000672.1:g.50690855G= GRCh37
NC_000010.9:g.50360861G= NCBI36
NG_009442.1:g.61293C= , LRG_465:g.61293C=

Transcript Alleles

HGVS Amino-acid Change
NM_000124.4:c.2047C= MANE Select NP_000115.1:p.Arg683=
ENST00000355832.10:c.2047C= MANE Select ENSP00000348089.5:p.Arg683=
NM_000124.3:c.2047C= NP_000115.1:p.Arg683=
NM_001346440.1:c.2047C= NP_001333369.1:p.Arg683=
NM_001346440.2:c.2047C= NP_001333369.1:p.Arg683=
ENST00000355832.9:c.2047C= ENSP00000348089.5:p.Arg683=
ENST00000623073.3:c.*439C= ENSP00000485650.1:n.*439C=
ENST00000623115.3:c.157C= ENSP00000485321.1:p.Arg53=
ENST00000681632.1:n.2125C=
ENST00000681659.1:c.1888C= ENSP00000505631.1:p.Arg630=