Canonical Allele Identifier: CA376708776

Gene: ERCC6

Linked Data

• ClinVar Variation Id: 2122419
• ClinVar RCV Id: RCV003054038
• MyVariant Identifiers: chr10:g.50669590C>G (hg19) ; chr10:g.49461544C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461544C>G , CM000672.2:g.49461544C>G	GRCh38
NC_000010.10:g.50669590C>G , CM000672.1:g.50669590C>G	GRCh37
NC_000010.9:g.50339596C>G	NCBI36
NG_009442.1:g.82558G>C , LRG_465:g.82558G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3791G>C MANE Select	ENSP00000348089.5:p.Ser1264Thr
ENST00000679552.1:n.862G>C
ENST00000679871.1:n.937G>C
ENST00000679974.1:n.840G>C
ENST00000681632.1:n.5194G>C
ENST00000681659.1:c.3632G>C	ENSP00000505631.1:p.Ser1211Thr
ENST00000355832.9:c.3791G>C	ENSP00000348089.5:p.Ser1264Thr
ENST00000465653.1:n.113G>C
ENST00000623073.3:c.*2087G>C	ENSP00000485650.1:n.*2087G>C
ENST00000623115.3:c.1901G>C	ENSP00000485321.1:p.Ser634Thr
ENST00000624341.3:c.1623G>C
NM_000124.3:c.3791G>C	NP_000115.1:p.Ser1264Thr
XR_945953.1:n.243-10021C>G
NM_001346440.1:c.3791G>C	NP_001333369.1:p.Ser1264Thr
NM_000124.4:c.3791G>C MANE Select	NP_000115.1:p.Ser1264Thr
NM_001346440.2:c.3791G>C	NP_001333369.1:p.Ser1264Thr