Canonical Allele Identifier: CA376717882

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50679149A>C (hg19) ; chr10:g.49471103A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49471103A>C , CM000672.2:g.49471103A>C	GRCh38
NC_000010.10:g.50679149A>C , CM000672.1:g.50679149A>C	GRCh37
NC_000010.9:g.50349155A>C	NCBI36
NG_009442.1:g.72999T>G , LRG_465:g.72999T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.2942T>G MANE Select	ENSP00000348089.5:p.Phe981Cys
ENST00000679552.1:n.142-214T>G
ENST00000679871.1:n.88T>G
ENST00000679974.1:n.120-214T>G
ENST00000681632.1:n.4345T>G
ENST00000681659.1:c.2783T>G	ENSP00000505631.1:p.Phe928Cys
ENST00000355832.9:c.2942T>G	ENSP00000348089.5:p.Phe981Cys
ENST00000623073.3:c.*1238T>G	ENSP00000485650.1:n.*1238T>G
ENST00000623115.3:c.1052T>G	ENSP00000485321.1:p.Phe351Cys
ENST00000624341.3:c.774T>G
NM_000124.3:c.2942T>G	NP_000115.1:p.Phe981Cys
XR_945953.1:n.243-462A>C
NM_001346440.1:c.2942T>G	NP_001333369.1:p.Phe981Cys
NM_000124.4:c.2942T>G MANE Select	NP_000115.1:p.Phe981Cys
NM_001346440.2:c.2942T>G	NP_001333369.1:p.Phe981Cys