Canonical Allele Identifier: CA376717333

Gene: ERCC6

Linked Data

• gnomAD v4: 10-49470988-A-C
• MyVariant Identifiers: chr10:g.50679034A>C (hg19) ; chr10:g.49470988A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470988A>C , CM000672.2:g.49470988A>C	GRCh38
NC_000010.10:g.50679034A>C , CM000672.1:g.50679034A>C	GRCh37
NC_000010.9:g.50349040A>C	NCBI36
NG_009442.1:g.73114T>G , LRG_465:g.73114T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3057T>G MANE Select	ENSP00000348089.5:p.Ser1019Arg
ENST00000679552.1:n.142-99T>G
ENST00000679871.1:n.203T>G
ENST00000679974.1:n.120-99T>G
ENST00000681632.1:n.4460T>G
ENST00000681659.1:c.2898T>G	ENSP00000505631.1:p.Ser966Arg
ENST00000355832.9:c.3057T>G	ENSP00000348089.5:p.Ser1019Arg
ENST00000623073.3:c.*1353T>G	ENSP00000485650.1:n.*1353T>G
ENST00000623115.3:c.1167T>G	ENSP00000485321.1:p.Ser389Arg
ENST00000624341.3:c.889T>G
NM_000124.3:c.3057T>G	NP_000115.1:p.Ser1019Arg
XR_945953.1:n.243-577A>C
NM_001346440.1:c.3057T>G	NP_001333369.1:p.Ser1019Arg
NM_000124.4:c.3057T>G MANE Select	NP_000115.1:p.Ser1019Arg
NM_001346440.2:c.3057T>G	NP_001333369.1:p.Ser1019Arg