Canonical Allele Identifier: CA376708341

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50669471A>G (hg19) ; chr10:g.49461425A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461425A>G , CM000672.2:g.49461425A>G	GRCh38
NC_000010.10:g.50669471A>G , CM000672.1:g.50669471A>G	GRCh37
NC_000010.9:g.50339477A>G	NCBI36
NG_009442.1:g.82677T>C , LRG_465:g.82677T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3910T>C MANE Select	ENSP00000348089.5:p.Cys1304Arg
ENST00000679552.1:n.981T>C
ENST00000679871.1:n.1056T>C
ENST00000679974.1:n.959T>C
ENST00000681632.1:n.5313T>C
ENST00000681659.1:c.3751T>C	ENSP00000505631.1:p.Cys1251Arg
ENST00000355832.9:c.3910T>C	ENSP00000348089.5:p.Cys1304Arg
ENST00000465653.1:n.232T>C
ENST00000623073.3:c.*2206T>C	ENSP00000485650.1:n.*2206T>C
ENST00000623115.3:c.2020T>C	ENSP00000485321.1:p.Cys674Arg
ENST00000624341.3:c.1742T>C
NM_000124.3:c.3910T>C	NP_000115.1:p.Cys1304Arg
XR_945953.1:n.243-10140A>G
NM_001346440.1:c.3910T>C	NP_001333369.1:p.Cys1304Arg
NM_000124.4:c.3910T>C MANE Select	NP_000115.1:p.Cys1304Arg
NM_001346440.2:c.3910T>C	NP_001333369.1:p.Cys1304Arg