Canonical Allele Identifier: CA1908749346
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49470326A= , CM000672.2:g.49470326A= GRCh38
NC_000010.10:g.50678372A= , CM000672.1:g.50678372A= GRCh37
NC_000010.9:g.50348378A= NCBI36
NG_009442.1:g.73776T= , LRG_465:g.73776T=

Transcript Alleles

HGVS Amino-acid change
ENST00000355832.10:c.3634T= MANE Select ENSP00000348089.5:p.Cys1212=
ENST00000679552.1:n.705T=
ENST00000679871.1:n.780T=
ENST00000679974.1:n.683T=
ENST00000681632.1:n.5037T=
ENST00000681659.1:c.3475T= ENSP00000505631.1:p.Cys1159=
ENST00000355832.9:c.3634T= ENSP00000348089.5:p.Cys1212=
ENST00000623073.3:c.*1930T= ENSP00000485650.1:n.*1930T=
ENST00000623115.3:c.1744T= ENSP00000485321.1:p.Cys582=
ENST00000624341.3:c.1466T=
NM_000124.3:c.3634T= NP_000115.1:p.Cys1212=
XR_945953.1:n.243-1239A=
NM_001346440.1:c.3634T= NP_001333369.1:p.Cys1212=
NM_000124.4:c.3634T= MANE Select NP_000115.1:p.Cys1212=
NM_001346440.2:c.3634T= NP_001333369.1:p.Cys1212=