Canonical Allele Identifier: CA469789122

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50678829A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470783A>T , CM000672.2:g.49470783A>T	GRCh38
NC_000010.10:g.50678829A>T , CM000672.1:g.50678829A>T	GRCh37
NC_000010.9:g.50348835A>T	NCBI36
NG_009442.1:g.73319T>A , LRG_465:g.73319T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3177T>A MANE Select	ENSP00000348089.5:p.Ser1059=
ENST00000679552.1:n.248T>A
ENST00000679871.1:n.323T>A
ENST00000679974.1:n.226T>A
ENST00000681632.1:n.4580T>A
ENST00000681659.1:c.3018T>A	ENSP00000505631.1:p.Ser1006=
ENST00000355832.9:c.3177T>A	ENSP00000348089.5:p.Ser1059=
ENST00000623073.3:c.*1473T>A	ENSP00000485650.1:n.*1473T>A
ENST00000623115.3:c.1287T>A	ENSP00000485321.1:p.Ser429=
ENST00000624341.3:c.1009T>A
NM_000124.3:c.3177T>A	NP_000115.1:p.Ser1059=
XR_945953.1:n.243-782A>T
NM_001346440.1:c.3177T>A	NP_001333369.1:p.Ser1059=
NM_000124.4:c.3177T>A MANE Select	NP_000115.1:p.Ser1059=
NM_001346440.2:c.3177T>A	NP_001333369.1:p.Ser1059=