Canonical Allele Identifier: CA1908744533
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49459233T= , CM000672.2:g.49459233T= GRCh38
NC_000010.10:g.50667279T= , CM000672.1:g.50667279T= GRCh37
NC_000010.9:g.50337285T= NCBI36
NG_009442.1:g.84869A= , LRG_465:g.84869A=

Transcript Alleles

HGVS Amino-acid change
ENST00000355832.10:c.4064A= MANE Select ENSP00000348089.5:p.Asp1355=
ENST00000679552.1:n.2273A=
ENST00000679871.1:n.1210A=
ENST00000679974.1:n.1113A=
ENST00000681632.1:n.5467A=
ENST00000681659.1:c.3905A= ENSP00000505631.1:p.Asp1302=
ENST00000355832.9:c.4064A= ENSP00000348089.5:p.Asp1355=
ENST00000623073.3:c.*2360A= ENSP00000485650.1:n.*2360A=
ENST00000623115.3:c.2174A= ENSP00000485321.1:p.Asp725=
ENST00000624341.3:c.1896A=
NM_000124.3:c.4064A= NP_000115.1:p.Asp1355=
XR_945953.1:n.243-12332T=
NM_001346440.1:c.4064A= NP_001333369.1:p.Asp1355=
NM_000124.4:c.4064A= MANE Select NP_000115.1:p.Asp1355=
NM_001346440.2:c.4064A= NP_001333369.1:p.Asp1355=