Canonical Allele Identifier: CA10630906
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 362782
ClinVar RCV Id: RCV000364219
dbSNP Id: rs886062879

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31033755_31033756insG , CM000670.2:g.31033755_31033756insG GRCh38
NC_000008.10:g.30891271_30891272insG , CM000670.1:g.30891271_30891272insG GRCh37
NC_000008.9:g.31010813_31010814insG NCBI36
NG_008870.1:g.5494_5495insG , LRG_524:g.5494_5495insG

Transcript Alleles

HGVS Amino-acid Change
NM_000553.4:c.-295_-294insG , LRG_524t1:c.-295_-294insG NP_000544.2:n.-295_-294insG
NM_000553.5:c.-295_-294insG NP_000544.2:n.-295_-294insG
XM_011544639.3:c.-295_-294insG XP_011542941.1:n.-295_-294insG
XR_949470.3:n.7_8insG
XR_949471.3:n.7_8insG
XR_949472.3:n.7_8insG