Canonical Allele Identifier: CA1908778515
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49500593C= , CM000672.2:g.49500593C= GRCh38
NC_000010.10:g.50708639C= , CM000672.1:g.50708639C= GRCh37
NC_000010.9:g.50378645C= NCBI36
NG_009442.1:g.43509G= , LRG_465:g.43509G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355832.10:c.1630G= MANE Select ENSP00000348089.5:p.Ala544=
ENST00000681632.1:n.1708G=
ENST00000681659.1:c.1526+5291G= ENSP00000505631.1:n.1526+5291G=
ENST00000355832.9:c.1630G= ENSP00000348089.5:p.Ala544=
ENST00000475116.1:n.220G=
ENST00000623073.3:c.31G= ENSP00000485650.1:p.Ala11=
ENST00000623115.3:c.-125G= ENSP00000485321.1:n.-125G=
ENST00000623318.1:c.31G= ENSP00000485423.1:p.Ala11=
NM_000124.3:c.1630G= NP_000115.1:p.Ala544=
NM_001346440.1:c.1630G= NP_001333369.1:p.Ala544=
NM_000124.4:c.1630G= MANE Select NP_000115.1:p.Ala544=
NM_001346440.2:c.1630G= NP_001333369.1:p.Ala544=