Canonical Allele Identifier: CA5495889

Gene: ERCC6

Linked Data

• ClinVar Variation Id: 1093548
• ClinVar RCV Id: RCV001413738
• dbSNP Id: rs747836397
• ExAC: 10:50701283 A / C
• gnomAD v2: 10-50701283-A-C
• gnomAD v3: 10-49493237-A-C
• gnomAD v4: 10-49493237-A-C
• MyVariant Identifiers: chr10:g.50701283A>C (hg19) ; chr10:g.49493237A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49493237A>C , CM000672.2:g.49493237A>C	GRCh38
NC_000010.10:g.50701283A>C , CM000672.1:g.50701283A>C	GRCh37
NC_000010.9:g.50371289A>C	NCBI36
NG_009442.1:g.50865T>G , LRG_465:g.50865T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.1701T>G MANE Select	ENSP00000348089.5:p.Gly567=
ENST00000681632.1:n.1779T>G
ENST00000681659.1:c.1542T>G	ENSP00000505631.1:p.Gly514=
ENST00000355832.9:c.1701T>G	ENSP00000348089.5:p.Gly567=
ENST00000475116.1:n.275+7301T>G
ENST00000623073.3:c.102T>G	ENSP00000485650.1:p.Gly34=
ENST00000623115.3:c.-70+7301T>G	ENSP00000485321.1:n.-70+7301T>G
ENST00000623318.1:c.102T>G	ENSP00000485423.1:p.Gly34=
NM_000124.3:c.1701T>G	NP_000115.1:p.Gly567=
NM_001346440.1:c.1701T>G	NP_001333369.1:p.Gly567=
NM_000124.4:c.1701T>G MANE Select	NP_000115.1:p.Gly567=
NM_001346440.2:c.1701T>G	NP_001333369.1:p.Gly567=