Canonical Allele Identifier: CA5495652
Gene: ERCC6 HGNC NCBI
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49474234G>A , CM000672.2:g.49474234G>A GRCh38
NC_000010.10:g.50682280G>A , CM000672.1:g.50682280G>A GRCh37
NC_000010.9:g.50352286G>A NCBI36
NG_009442.1:g.69868C>T , LRG_465:g.69868C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355832.10:c.2391C>T MANE Select ENSP00000348089.5:p.Ser797=
ENST00000681632.1:n.2469C>T
ENST00000681659.1:c.2232C>T ENSP00000505631.1:p.Ser744=
ENST00000355832.9:c.2391C>T ENSP00000348089.5:p.Ser797=
ENST00000623073.3:c.*687C>T ENSP00000485650.1:n.*687C>T
ENST00000623115.3:c.501C>T ENSP00000485321.1:p.Ser167=
ENST00000624341.3:c.223C>T
NM_000124.3:c.2391C>T NP_000115.1:p.Ser797=
NM_001346440.1:c.2391C>T NP_001333369.1:p.Ser797=
NM_000124.4:c.2391C>T MANE Select NP_000115.1:p.Ser797=
NM_001346440.2:c.2391C>T NP_001333369.1:p.Ser797=