Canonical Allele Identifier: CA376714330

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50678510C>T (hg19) ; chr10:g.49470464C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470464C>T , CM000672.2:g.49470464C>T	GRCh38
NC_000010.10:g.50678510C>T , CM000672.1:g.50678510C>T	GRCh37
NC_000010.9:g.50348516C>T	NCBI36
NG_009442.1:g.73638G>A , LRG_465:g.73638G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3496G>A MANE Select	ENSP00000348089.5:p.Glu1166Lys
ENST00000679552.1:n.567G>A
ENST00000679871.1:n.642G>A
ENST00000679974.1:n.545G>A
ENST00000681632.1:n.4899G>A
ENST00000681659.1:c.3337G>A	ENSP00000505631.1:p.Glu1113Lys
ENST00000355832.9:c.3496G>A	ENSP00000348089.5:p.Glu1166Lys
ENST00000623073.3:c.*1792G>A	ENSP00000485650.1:n.*1792G>A
ENST00000623115.3:c.1606G>A	ENSP00000485321.1:p.Glu536Lys
ENST00000624341.3:c.1328G>A
NM_000124.3:c.3496G>A	NP_000115.1:p.Glu1166Lys
XR_945953.1:n.243-1101C>T
NM_001346440.1:c.3496G>A	NP_001333369.1:p.Glu1166Lys
NM_000124.4:c.3496G>A MANE Select	NP_000115.1:p.Glu1166Lys
NM_001346440.2:c.3496G>A	NP_001333369.1:p.Glu1166Lys