Canonical Allele Identifier: CA376717907

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50679158A>T (hg19) ; chr10:g.49471112A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49471112A>T , CM000672.2:g.49471112A>T	GRCh38
NC_000010.10:g.50679158A>T , CM000672.1:g.50679158A>T	GRCh37
NC_000010.9:g.50349164A>T	NCBI36
NG_009442.1:g.72990T>A , LRG_465:g.72990T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.2933T>A MANE Select	ENSP00000348089.5:p.Phe978Tyr
ENST00000679552.1:n.142-223T>A
ENST00000679871.1:n.79T>A
ENST00000679974.1:n.120-223T>A
ENST00000681632.1:n.4336T>A
ENST00000681659.1:c.2774T>A	ENSP00000505631.1:p.Phe925Tyr
ENST00000355832.9:c.2933T>A	ENSP00000348089.5:p.Phe978Tyr
ENST00000623073.3:c.*1229T>A	ENSP00000485650.1:n.*1229T>A
ENST00000623115.3:c.1043T>A	ENSP00000485321.1:p.Phe348Tyr
ENST00000624341.3:c.765T>A
NM_000124.3:c.2933T>A	NP_000115.1:p.Phe978Tyr
XR_945953.1:n.243-453A>T
NM_001346440.1:c.2933T>A	NP_001333369.1:p.Phe978Tyr
NM_000124.4:c.2933T>A MANE Select	NP_000115.1:p.Phe978Tyr
NM_001346440.2:c.2933T>A	NP_001333369.1:p.Phe978Tyr