Canonical Allele Identifier: CA2091759654
Gene: THSD1 HGNC NCBI

Linked Data

dbSNP Id: rs1957822609
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.52397738_52397740del , CM000675.2:g.52397738_52397740del GRCh38
NC_000013.10:g.52971873_52971875del , CM000675.1:g.52971873_52971875del GRCh37
NC_000013.9:g.51869874_51869876del NCBI36
NG_047168.1:g.13757_13759del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258613.5:c.515_517del MANE Select ENSP00000258613.4:p.Thr172del
ENST00000648254.1:c.515_517del ENSP00000497520.1:p.Thr172del
ENST00000258613.4:c.515_517del ENSP00000258613.4:p.Thr172del
ENST00000349258.8:c.515_517del ENSP00000340650.4:p.Thr172del
NM_018676.3:c.515_517del NP_061146.1:p.Thr172del
NM_199263.2:c.515_517del NP_954872.1:p.Thr172del
NM_018676.4:c.515_517del MANE Select NP_061146.1:p.Thr172del
NM_199263.3:c.515_517del NP_954872.1:p.Thr172del
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