Canonical Allele Identifier: CA376724385
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49482809G>C , CM000672.2:g.49482809G>C GRCh38
NC_000010.10:g.50690855G>C , CM000672.1:g.50690855G>C GRCh37
NC_000010.9:g.50360861G>C NCBI36
NG_009442.1:g.61293C>G , LRG_465:g.61293C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000124.4:c.2047C>G MANE Select NP_000115.1:p.Arg683Gly
ENST00000355832.10:c.2047C>G MANE Select ENSP00000348089.5:p.Arg683Gly
NM_000124.3:c.2047C>G NP_000115.1:p.Arg683Gly
NM_001346440.1:c.2047C>G NP_001333369.1:p.Arg683Gly
NM_001346440.2:c.2047C>G NP_001333369.1:p.Arg683Gly
ENST00000355832.9:c.2047C>G ENSP00000348089.5:p.Arg683Gly
ENST00000623073.3:c.*439C>G ENSP00000485650.1:n.*439C>G
ENST00000623115.3:c.157C>G ENSP00000485321.1:p.Arg53Gly
ENST00000681632.1:n.2125C>G
ENST00000681659.1:c.1888C>G ENSP00000505631.1:p.Arg630Gly