Canonical Allele Identifier: CA5496488

Gene: ERCC6

Linked Data

• ClinVar Variation Id: 1115537
• ClinVar RCV Id: RCV001443608
• dbSNP Id: rs140876119
• ExAC: 10:50736485 G / A
• gnomAD v2: 10-50736485-G-A
• gnomAD v3: 10-49528439-G-A
• gnomAD v4: 10-49528439-G-A
• COSMIC: COSM4014459
• MyVariant Identifiers: chr10:g.50736485G>A (hg19) ; chr10:g.49528439G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49528439G>A , CM000672.2:g.49528439G>A	GRCh38
NC_000010.10:g.50736485G>A , CM000672.1:g.50736485G>A	GRCh37
NC_000010.9:g.50406491G>A	NCBI36
NG_009442.1:g.15663C>T , LRG_465:g.15663C>T
NG_033155.1:g.843C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.630C>T MANE Select	ENSP00000348089.5:p.His210=
ENST00000447839.7:c.630C>T MANE Plus Clinical	ENSP00000387966.2:p.His210=
ENST00000679596.1:c.*259C>T	ENSP00000504862.1:n.*259C>T
ENST00000679811.1:n.713C>T
ENST00000680107.1:c.630C>T	ENSP00000505909.1:p.His210=
ENST00000680233.1:n.723C>T
ENST00000681632.1:n.708C>T
ENST00000681659.1:c.630C>T	ENSP00000505631.1:p.His210=
ENST00000355832.9:c.630C>T	ENSP00000348089.5:p.His210=
ENST00000447839.6:c.630C>T	ENSP00000387966.2:p.His210=
ENST00000479652.1:n.105C>T
ENST00000515869.1:c.630C>T	ENSP00000423550.1:p.His210=
NM_000124.3:c.630C>T	NP_000115.1:p.His210=
NM_001277058.1:c.630C>T	NP_001263987.1:p.His210=
NM_001277059.1:c.630C>T	NP_001263988.1:p.His210=
NM_001346440.1:c.630C>T	NP_001333369.1:p.His210=
NM_000124.4:c.630C>T MANE Select	NP_000115.1:p.His210=
NM_001277058.2:c.630C>T MANE Plus Clinical	NP_001263987.1:p.His210=
NM_001277059.2:c.630C>T	NP_001263988.1:p.His210=
NM_001346440.2:c.630C>T	NP_001333369.1:p.His210=