Canonical Allele Identifier: CA5495393

Gene: ERCC6

Linked Data

• ClinVar Variation Id: 1163516
• ClinVar RCV Id: RCV001508656
• dbSNP Id: rs148475034
• ExAC: 10:50678819 C / T
• gnomAD v2: 10-50678819-C-T
• gnomAD v3: 10-49470773-C-T
• gnomAD v4: 10-49470773-C-T
• MyVariant Identifiers: chr10:g.50678819C>T (hg19) ; chr10:g.49470773C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470773C>T , CM000672.2:g.49470773C>T	GRCh38
NC_000010.10:g.50678819C>T , CM000672.1:g.50678819C>T	GRCh37
NC_000010.9:g.50348825C>T	NCBI36
NG_009442.1:g.73329G>A , LRG_465:g.73329G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3187G>A MANE Select	ENSP00000348089.5:p.Val1063Ile
ENST00000679552.1:n.258G>A
ENST00000679871.1:n.333G>A
ENST00000679974.1:n.236G>A
ENST00000681632.1:n.4590G>A
ENST00000681659.1:c.3028G>A	ENSP00000505631.1:p.Val1010Ile
ENST00000355832.9:c.3187G>A	ENSP00000348089.5:p.Val1063Ile
ENST00000623073.3:c.*1483G>A	ENSP00000485650.1:n.*1483G>A
ENST00000623115.3:c.1297G>A	ENSP00000485321.1:p.Val433Ile
ENST00000624341.3:c.1019G>A
NM_000124.3:c.3187G>A	NP_000115.1:p.Val1063Ile
XR_945953.1:n.243-792C>T
NM_001346440.1:c.3187G>A	NP_001333369.1:p.Val1063Ile
NM_000124.4:c.3187G>A MANE Select	NP_000115.1:p.Val1063Ile
NM_001346440.2:c.3187G>A	NP_001333369.1:p.Val1063Ile