Canonical Allele Identifier: CA2091759546
Gene: THSD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.52397635A= , CM000675.2:g.52397635A= GRCh38
NC_000013.10:g.52971770A= , CM000675.1:g.52971770A= GRCh37
NC_000013.9:g.51869771A= NCBI36
NG_047168.1:g.13860T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258613.5:c.618T= MANE Select ENSP00000258613.4:p.Cys206=
ENST00000648254.1:c.618T= ENSP00000497520.1:p.Cys206=
ENST00000258613.4:c.618T= ENSP00000258613.4:p.Cys206=
ENST00000349258.8:c.618T= ENSP00000340650.4:p.Cys206=
NM_018676.3:c.618T= NP_061146.1:p.Cys206=
NM_199263.2:c.618T= NP_954872.1:p.Cys206=
NM_018676.4:c.618T= MANE Select NP_061146.1:p.Cys206=
NM_199263.3:c.618T= NP_954872.1:p.Cys206=