Canonical Allele Identifier: CA388036790
Gene: THSD1 HGNC NCBI

Linked Data

dbSNP Id: rs1293813714

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.52397450A>G , CM000675.2:g.52397450A>G GRCh38
NC_000013.10:g.52971585A>G , CM000675.1:g.52971585A>G GRCh37
NC_000013.9:g.51869586A>G NCBI36
NG_047168.1:g.14045T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258613.5:c.803T>C MANE Select ENSP00000258613.4:p.Val268Ala
ENST00000648254.1:c.803T>C ENSP00000497520.1:p.Val268Ala
ENST00000258613.4:c.803T>C ENSP00000258613.4:p.Val268Ala
ENST00000349258.8:c.803T>C ENSP00000340650.4:p.Val268Ala
NM_018676.3:c.803T>C NP_061146.1:p.Val268Ala
NM_199263.2:c.803T>C NP_954872.1:p.Val268Ala
NM_018676.4:c.803T>C MANE Select NP_061146.1:p.Val268Ala
NM_199263.3:c.803T>C NP_954872.1:p.Val268Ala