Canonical Allele Identifier: CA469604487
Gene: ERCC6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1609865
ClinVar RCV Id: RCV002152742
dbSNP Id: rs1851205258
MyVariant Identifiers: chr10:g.50701178G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49493132G>A , CM000672.2:g.49493132G>A GRCh38
NC_000010.10:g.50701178G>A , CM000672.1:g.50701178G>A GRCh37
NC_000010.9:g.50371184G>A NCBI36
NG_009442.1:g.50970C>T , LRG_465:g.50970C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355832.10:c.1806C>T MANE Select ENSP00000348089.5:p.Ser602=
ENST00000681632.1:n.1884C>T
ENST00000681659.1:c.1647C>T ENSP00000505631.1:p.Ser549=
ENST00000355832.9:c.1806C>T ENSP00000348089.5:p.Ser602=
ENST00000475116.1:n.275+7406C>T
ENST00000623073.3:c.207C>T ENSP00000485650.1:p.Ser69=
ENST00000623115.3:c.-70+7406C>T ENSP00000485321.1:n.-70+7406C>T
ENST00000623318.1:c.207C>T ENSP00000485423.1:p.Ser69=
NM_000124.3:c.1806C>T NP_000115.1:p.Ser602=
NM_001346440.1:c.1806C>T NP_001333369.1:p.Ser602=
NM_000124.4:c.1806C>T MANE Select NP_000115.1:p.Ser602=
NM_001346440.2:c.1806C>T NP_001333369.1:p.Ser602=