Canonical Allele Identifier: CA1908749352
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49470333A= , CM000672.2:g.49470333A= GRCh38
NC_000010.10:g.50678379A= , CM000672.1:g.50678379A= GRCh37
NC_000010.9:g.50348385A= NCBI36
NG_009442.1:g.73769T= , LRG_465:g.73769T=

Transcript Alleles

HGVS Amino-acid change
ENST00000355832.10:c.3627T= MANE Select ENSP00000348089.5:p.Ser1209=
ENST00000679552.1:n.698T=
ENST00000679871.1:n.773T=
ENST00000679974.1:n.676T=
ENST00000681632.1:n.5030T=
ENST00000681659.1:c.3468T= ENSP00000505631.1:p.Ser1156=
ENST00000355832.9:c.3627T= ENSP00000348089.5:p.Ser1209=
ENST00000623073.3:c.*1923T= ENSP00000485650.1:n.*1923T=
ENST00000623115.3:c.1737T= ENSP00000485321.1:p.Ser579=
ENST00000624341.3:c.1459T=
NM_000124.3:c.3627T= NP_000115.1:p.Ser1209=
XR_945953.1:n.243-1232A=
NM_001346440.1:c.3627T= NP_001333369.1:p.Ser1209=
NM_000124.4:c.3627T= MANE Select NP_000115.1:p.Ser1209=
NM_001346440.2:c.3627T= NP_001333369.1:p.Ser1209=