Canonical Allele Identifier: CA5495255

Gene: ERCC6

Linked Data

• ClinVar Variation Id: 2159371
• ClinVar RCV Id: RCV003085929
• dbSNP Id: rs778477262
• ExAC: 10:50669549 C / T
• gnomAD v2: 10-50669549-C-T
• gnomAD v3: 10-49461503-C-T
• gnomAD v4: 10-49461503-C-T
• MyVariant Identifiers: chr10:g.50669549C>T (hg19) ; chr10:g.49461503C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461503C>T , CM000672.2:g.49461503C>T	GRCh38
NC_000010.10:g.50669549C>T , CM000672.1:g.50669549C>T	GRCh37
NC_000010.9:g.50339555C>T	NCBI36
NG_009442.1:g.82599G>A , LRG_465:g.82599G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3832G>A MANE Select	ENSP00000348089.5:p.Asp1278Asn
ENST00000679552.1:n.903G>A
ENST00000679871.1:n.978G>A
ENST00000679974.1:n.881G>A
ENST00000681632.1:n.5235G>A
ENST00000681659.1:c.3673G>A	ENSP00000505631.1:p.Asp1225Asn
ENST00000355832.9:c.3832G>A	ENSP00000348089.5:p.Asp1278Asn
ENST00000465653.1:n.154G>A
ENST00000623073.3:c.*2128G>A	ENSP00000485650.1:n.*2128G>A
ENST00000623115.3:c.1942G>A	ENSP00000485321.1:p.Asp648Asn
ENST00000624341.3:c.1664G>A
NM_000124.3:c.3832G>A	NP_000115.1:p.Asp1278Asn
XR_945953.1:n.243-10062C>T
NM_001346440.1:c.3832G>A	NP_001333369.1:p.Asp1278Asn
NM_000124.4:c.3832G>A MANE Select	NP_000115.1:p.Asp1278Asn
NM_001346440.2:c.3832G>A	NP_001333369.1:p.Asp1278Asn