Canonical Allele Identifier: CA1908760559
Community Standard Title: NM_000124.4(ERCC6):c.2008C= (p.Arg670=)
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49482848G= , CM000672.2:g.49482848G= GRCh38
NC_000010.10:g.50690894G= , CM000672.1:g.50690894G= GRCh37
NC_000010.9:g.50360900G= NCBI36
NG_009442.1:g.61254C= , LRG_465:g.61254C=

Transcript Alleles

HGVS Amino-acid Change
NM_000124.4:c.2008C= MANE Select NP_000115.1:p.Arg670=
ENST00000355832.10:c.2008C= MANE Select ENSP00000348089.5:p.Arg670=
NM_000124.3:c.2008C= NP_000115.1:p.Arg670=
NM_001346440.1:c.2008C= NP_001333369.1:p.Arg670=
NM_001346440.2:c.2008C= NP_001333369.1:p.Arg670=
ENST00000355832.9:c.2008C= ENSP00000348089.5:p.Arg670=
ENST00000623073.3:c.*400C= ENSP00000485650.1:n.*400C=
ENST00000623115.3:c.118C= ENSP00000485321.1:p.Arg40=
ENST00000681632.1:n.2086C=
ENST00000681659.1:c.1849C= ENSP00000505631.1:p.Arg617=