Canonical Allele Identifier: CA376716079

Gene: ERCC6

Linked Data

• gnomAD v4: 10-49470697-C-T
• MyVariant Identifiers: chr10:g.50678743C>T (hg19) ; chr10:g.49470697C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470697C>T , CM000672.2:g.49470697C>T	GRCh38
NC_000010.10:g.50678743C>T , CM000672.1:g.50678743C>T	GRCh37
NC_000010.9:g.50348749C>T	NCBI36
NG_009442.1:g.73405G>A , LRG_465:g.73405G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3263G>A MANE Select	ENSP00000348089.5:p.Ser1088Asn
ENST00000679552.1:n.334G>A
ENST00000679871.1:n.409G>A
ENST00000679974.1:n.312G>A
ENST00000681632.1:n.4666G>A
ENST00000681659.1:c.3104G>A	ENSP00000505631.1:p.Ser1035Asn
ENST00000355832.9:c.3263G>A	ENSP00000348089.5:p.Ser1088Asn
ENST00000623073.3:c.*1559G>A	ENSP00000485650.1:n.*1559G>A
ENST00000623115.3:c.1373G>A	ENSP00000485321.1:p.Ser458Asn
ENST00000624341.3:c.1095G>A
NM_000124.3:c.3263G>A	NP_000115.1:p.Ser1088Asn
XR_945953.1:n.243-868C>T
NM_001346440.1:c.3263G>A	NP_001333369.1:p.Ser1088Asn
NM_000124.4:c.3263G>A MANE Select	NP_000115.1:p.Ser1088Asn
NM_001346440.2:c.3263G>A	NP_001333369.1:p.Ser1088Asn