Canonical Allele Identifier: CA388039092
Gene: THSD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.52397875T>A , CM000675.2:g.52397875T>A GRCh38
NC_000013.10:g.52972010T>A , CM000675.1:g.52972010T>A GRCh37
NC_000013.9:g.51870011T>A NCBI36
NG_047168.1:g.13620A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258613.5:c.378A>T MANE Select ENSP00000258613.4:p.Glu126Asp
ENST00000648254.1:c.378A>T ENSP00000497520.1:p.Glu126Asp
ENST00000258613.4:c.378A>T ENSP00000258613.4:p.Glu126Asp
ENST00000349258.8:c.378A>T ENSP00000340650.4:p.Glu126Asp
NM_018676.3:c.378A>T NP_061146.1:p.Glu126Asp
NM_199263.2:c.378A>T NP_954872.1:p.Glu126Asp
NM_018676.4:c.378A>T MANE Select NP_061146.1:p.Glu126Asp
NM_199263.3:c.378A>T NP_954872.1:p.Glu126Asp