Canonical Allele Identifier: CA388037419
Gene: THSD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.52397615G>T , CM000675.2:g.52397615G>T GRCh38
NC_000013.10:g.52971750G>T , CM000675.1:g.52971750G>T GRCh37
NC_000013.9:g.51869751G>T NCBI36
NG_047168.1:g.13880C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258613.5:c.638C>A MANE Select ENSP00000258613.4:p.Ala213Asp
ENST00000648254.1:c.638C>A ENSP00000497520.1:p.Ala213Asp
ENST00000258613.4:c.638C>A ENSP00000258613.4:p.Ala213Asp
ENST00000349258.8:c.638C>A ENSP00000340650.4:p.Ala213Asp
NM_018676.3:c.638C>A NP_061146.1:p.Ala213Asp
NM_199263.2:c.638C>A NP_954872.1:p.Ala213Asp
NM_018676.4:c.638C>A MANE Select NP_061146.1:p.Ala213Asp
NM_199263.3:c.638C>A NP_954872.1:p.Ala213Asp