Canonical Allele Identifier: CA376708368

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50669488C>T (hg19) ; chr10:g.49461442C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461442C>T , CM000672.2:g.49461442C>T	GRCh38
NC_000010.10:g.50669488C>T , CM000672.1:g.50669488C>T	GRCh37
NC_000010.9:g.50339494C>T	NCBI36
NG_009442.1:g.82660G>A , LRG_465:g.82660G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3893G>A MANE Select	ENSP00000348089.5:p.Arg1298Lys
ENST00000679552.1:n.964G>A
ENST00000679871.1:n.1039G>A
ENST00000679974.1:n.942G>A
ENST00000681632.1:n.5296G>A
ENST00000681659.1:c.3734G>A	ENSP00000505631.1:p.Arg1245Lys
ENST00000355832.9:c.3893G>A	ENSP00000348089.5:p.Arg1298Lys
ENST00000465653.1:n.215G>A
ENST00000623073.3:c.*2189G>A	ENSP00000485650.1:n.*2189G>A
ENST00000623115.3:c.2003G>A	ENSP00000485321.1:p.Arg668Lys
ENST00000624341.3:c.1725G>A
NM_000124.3:c.3893G>A	NP_000115.1:p.Arg1298Lys
XR_945953.1:n.243-10123C>T
NM_001346440.1:c.3893G>A	NP_001333369.1:p.Arg1298Lys
NM_000124.4:c.3893G>A MANE Select	NP_000115.1:p.Arg1298Lys
NM_001346440.2:c.3893G>A	NP_001333369.1:p.Arg1298Lys