Canonical Allele Identifier: CA919273233
Gene: THSD1 HGNC NCBI

Linked Data

dbSNP Id: rs1566074528

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.52397420del , CM000675.2:g.52397420del GRCh38
NC_000013.10:g.52971555del , CM000675.1:g.52971555del GRCh37
NC_000013.9:g.51869556del NCBI36
NG_047168.1:g.14079del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258613.5:c.837del MANE Select ENSP00000258613.4:p.Arg280AspfsTer?
ENST00000648254.1:c.837del ENSP00000497520.1:p.Arg280AspfsTer?
ENST00000258613.4:c.837del ENSP00000258613.4:p.Arg280AspfsTer?
ENST00000349258.8:c.837del ENSP00000340650.4:p.Arg280AspfsTer?
NM_018676.3:c.837del NP_061146.1:p.Arg280AspfsTer?
NM_199263.2:c.837del NP_954872.1:p.Arg280AspfsTer?
NM_018676.4:c.837del MANE Select NP_061146.1:p.Arg280AspfsTer?
NM_199263.3:c.837del NP_954872.1:p.Arg280AspfsTer?