Canonical Allele Identifier: CA174888590
Gene: WRN HGNC NCBI

Linked Data

dbSNP Id: rs5890546

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31033776del , CM000670.2:g.31033776del GRCh38
NC_000008.10:g.30891292del , CM000670.1:g.30891292del GRCh37
NC_000008.9:g.31010834del NCBI36
NG_008870.1:g.5515del , LRG_524:g.5515del

Transcript Alleles

HGVS Amino-acid Change
NM_000553.4:c.-274del , LRG_524t1:c.-274del NP_000544.2:n.-274del
NM_000553.5:c.-274del NP_000544.2:n.-274del
XM_011544639.3:c.-274del XP_011542941.1:n.-274del
XR_949470.3:n.28del
XR_949471.3:n.28del
XR_949472.3:n.28del