Canonical Allele Identifier: CA376708494

Gene: ERCC6

Linked Data

• gnomAD v4: 10-49461488-C-A
• MyVariant Identifiers: chr10:g.50669534C>A (hg19) ; chr10:g.49461488C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461488C>A , CM000672.2:g.49461488C>A	GRCh38
NC_000010.10:g.50669534C>A , CM000672.1:g.50669534C>A	GRCh37
NC_000010.9:g.50339540C>A	NCBI36
NG_009442.1:g.82614G>T , LRG_465:g.82614G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3847G>T MANE Select	ENSP00000348089.5:p.Glu1283Ter
ENST00000679552.1:n.918G>T
ENST00000679871.1:n.993G>T
ENST00000679974.1:n.896G>T
ENST00000681632.1:n.5250G>T
ENST00000681659.1:c.3688G>T	ENSP00000505631.1:p.Glu1230Ter
ENST00000355832.9:c.3847G>T	ENSP00000348089.5:p.Glu1283Ter
ENST00000465653.1:n.169G>T
ENST00000623073.3:c.*2143G>T	ENSP00000485650.1:n.*2143G>T
ENST00000623115.3:c.1957G>T	ENSP00000485321.1:p.Glu653Ter
ENST00000624341.3:c.1679G>T
NM_000124.3:c.3847G>T	NP_000115.1:p.Glu1283Ter
XR_945953.1:n.243-10077C>A
NM_001346440.1:c.3847G>T	NP_001333369.1:p.Glu1283Ter
NM_000124.4:c.3847G>T MANE Select	NP_000115.1:p.Glu1283Ter
NM_001346440.2:c.3847G>T	NP_001333369.1:p.Glu1283Ter