Canonical Allele Identifier: CA376708279

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50669439C>G (hg19) ; chr10:g.49461393C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461393C>G , CM000672.2:g.49461393C>G	GRCh38
NC_000010.10:g.50669439C>G , CM000672.1:g.50669439C>G	GRCh37
NC_000010.9:g.50339445C>G	NCBI36
NG_009442.1:g.82709G>C , LRG_465:g.82709G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3942G>C MANE Select	ENSP00000348089.5:p.Trp1314Cys
ENST00000679552.1:n.1013G>C
ENST00000679871.1:n.1088G>C
ENST00000679974.1:n.991G>C
ENST00000681632.1:n.5345G>C
ENST00000681659.1:c.3783G>C	ENSP00000505631.1:p.Trp1261Cys
ENST00000355832.9:c.3942G>C	ENSP00000348089.5:p.Trp1314Cys
ENST00000465653.1:n.264G>C
ENST00000623073.3:c.*2238G>C	ENSP00000485650.1:n.*2238G>C
ENST00000623115.3:c.2052G>C	ENSP00000485321.1:p.Trp684Cys
ENST00000624341.3:c.1774G>C
NM_000124.3:c.3942G>C	NP_000115.1:p.Trp1314Cys
XR_945953.1:n.243-10172C>G
NM_001346440.1:c.3942G>C	NP_001333369.1:p.Trp1314Cys
NM_000124.4:c.3942G>C MANE Select	NP_000115.1:p.Trp1314Cys
NM_001346440.2:c.3942G>C	NP_001333369.1:p.Trp1314Cys