Canonical Allele Identifier: CA347453
Gene: DVL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 208048
ClinVar RCV Id: RCV000195217
dbSNP Id: rs797044838

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1338089del , CM000663.2:g.1338089del GRCh38
NC_000001.10:g.1273469del , CM000663.1:g.1273469del GRCh37
NC_000001.9:g.1263332del NCBI36
NG_008048.1:g.16026del
NG_008048.2:g.16026del

Transcript Alleles

HGVS Amino-acid change
ENST00000378888.10:c.1604del MANE Select ENSP00000368166.5:p.Gly535ValfsTer?
ENST00000378888.9:c.1604del ENSP00000368166.5:p.Gly535ValfsTer?
ENST00000378891.9:c.1529del ENSP00000368169.5:p.Gly510ValfsTer?
ENST00000610709.2:c.851del ENSP00000480077.1:p.Gly284ValfsTer?
ENST00000631679.1:c.635del ENSP00000488181.1:p.Gly212ValfsTer?
ENST00000632445.1:c.533del ENSP00000488888.1:p.Gly178ValfsTer?
NM_004421.2:c.1529del NP_004412.2:p.Gly510ValfsTer?
XM_005244731.2:c.1604del XP_005244788.1:p.Gly535ValfsTer?
XM_005244732.2:c.1604del XP_005244789.1:p.Gly535ValfsTer?
XM_005244733.2:c.1529del XP_005244790.1:p.Gly510ValfsTer?
NM_001330311.1:c.1604del NP_001317240.1:p.Gly535ValfsTer?
XM_005244732.4:c.1604del XP_005244789.1:p.Gly535ValfsTer?
XM_005244733.4:c.1529del XP_005244790.1:p.Gly510ValfsTer?
NM_001330311.2:c.1604del MANE Select NP_001317240.1:p.Gly535ValfsTer?
NM_004421.3:c.1529del NP_004412.2:p.Gly510ValfsTer?