Canonical Allele Identifier: CA388039290
Gene: THSD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.52397904A>C , CM000675.2:g.52397904A>C GRCh38
NC_000013.10:g.52972039A>C , CM000675.1:g.52972039A>C GRCh37
NC_000013.9:g.51870040A>C NCBI36
NG_047168.1:g.13591T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258613.5:c.349T>G MANE Select ENSP00000258613.4:p.Trp117Gly
ENST00000648254.1:c.349T>G ENSP00000497520.1:p.Trp117Gly
ENST00000258613.4:c.349T>G ENSP00000258613.4:p.Trp117Gly
ENST00000349258.8:c.349T>G ENSP00000340650.4:p.Trp117Gly
NM_018676.3:c.349T>G NP_061146.1:p.Trp117Gly
NM_199263.2:c.349T>G NP_954872.1:p.Trp117Gly
NM_018676.4:c.349T>G MANE Select NP_061146.1:p.Trp117Gly
NM_199263.3:c.349T>G NP_954872.1:p.Trp117Gly