Canonical Allele Identifier: CA376713196

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50678373A>T (hg19) ; chr10:g.49470327A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470327A>T , CM000672.2:g.49470327A>T	GRCh38
NC_000010.10:g.50678373A>T , CM000672.1:g.50678373A>T	GRCh37
NC_000010.9:g.50348379A>T	NCBI36
NG_009442.1:g.73775T>A , LRG_465:g.73775T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.3633T>A MANE Select	ENSP00000348089.5:p.His1211Gln
ENST00000679552.1:n.704T>A
ENST00000679871.1:n.779T>A
ENST00000679974.1:n.682T>A
ENST00000681632.1:n.5036T>A
ENST00000681659.1:c.3474T>A	ENSP00000505631.1:p.His1158Gln
ENST00000355832.9:c.3633T>A	ENSP00000348089.5:p.His1211Gln
ENST00000623073.3:c.*1929T>A	ENSP00000485650.1:n.*1929T>A
ENST00000623115.3:c.1743T>A	ENSP00000485321.1:p.His581Gln
ENST00000624341.3:c.1465T>A
NM_000124.3:c.3633T>A	NP_000115.1:p.His1211Gln
XR_945953.1:n.243-1238A>T
NM_001346440.1:c.3633T>A	NP_001333369.1:p.His1211Gln
NM_000124.4:c.3633T>A MANE Select	NP_000115.1:p.His1211Gln
NM_001346440.2:c.3633T>A	NP_001333369.1:p.His1211Gln