Canonical Allele Identifier: CA1908745512
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49461475T= , CM000672.2:g.49461475T= GRCh38
NC_000010.10:g.50669521T= , CM000672.1:g.50669521T= GRCh37
NC_000010.9:g.50339527T= NCBI36
NG_009442.1:g.82627A= , LRG_465:g.82627A=

Transcript Alleles

HGVS Amino-acid change
ENST00000355832.10:c.3860A= MANE Select ENSP00000348089.5:p.Asn1287=
ENST00000679552.1:n.931A=
ENST00000679871.1:n.1006A=
ENST00000679974.1:n.909A=
ENST00000681632.1:n.5263A=
ENST00000681659.1:c.3701A= ENSP00000505631.1:p.Asn1234=
ENST00000355832.9:c.3860A= ENSP00000348089.5:p.Asn1287=
ENST00000465653.1:n.182A=
ENST00000623073.3:c.*2156A= ENSP00000485650.1:n.*2156A=
ENST00000623115.3:c.1970A= ENSP00000485321.1:p.Asn657=
ENST00000624341.3:c.1692A=
NM_000124.3:c.3860A= NP_000115.1:p.Asn1287=
XR_945953.1:n.243-10090T=
NM_001346440.1:c.3860A= NP_001333369.1:p.Asn1287=
NM_000124.4:c.3860A= MANE Select NP_000115.1:p.Asn1287=
NM_001346440.2:c.3860A= NP_001333369.1:p.Asn1287=