Canonical Allele Identifier: CA388036793

Gene: THSD1

Linked Data

• MyVariant Identifiers: chr13:g.52971586C>A (hg19) ; chr13:g.52397451C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.52397451C>A , CM000675.2:g.52397451C>A	GRCh38
NC_000013.10:g.52971586C>A , CM000675.1:g.52971586C>A	GRCh37
NC_000013.9:g.51869587C>A	NCBI36
NG_047168.1:g.14044G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258613.5:c.802G>T MANE Select	ENSP00000258613.4:p.Val268Phe
ENST00000648254.1:c.802G>T	ENSP00000497520.1:p.Val268Phe
ENST00000258613.4:c.802G>T	ENSP00000258613.4:p.Val268Phe
ENST00000349258.8:c.802G>T	ENSP00000340650.4:p.Val268Phe
NM_018676.3:c.802G>T	NP_061146.1:p.Val268Phe
NM_199263.2:c.802G>T	NP_954872.1:p.Val268Phe
NM_018676.4:c.802G>T MANE Select	NP_061146.1:p.Val268Phe
NM_199263.3:c.802G>T	NP_954872.1:p.Val268Phe