Canonical Allele Identifier: CA919273234

Gene: THSD1

Linked Data

• dbSNP Id: rs1566074573

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.52397461_52397471del , CM000675.2:g.52397461_52397471del	GRCh38
NC_000013.10:g.52971596_52971606del , CM000675.1:g.52971596_52971606del	GRCh37
NC_000013.9:g.51869597_51869607del	NCBI36
NG_047168.1:g.14027_14037del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258613.5:c.785_795del MANE Select	ENSP00000258613.4:p.Pro262HisfsTer26
ENST00000648254.1:c.785_795del	ENSP00000497520.1:p.Pro262HisfsTer26
ENST00000258613.4:c.785_795del	ENSP00000258613.4:p.Pro262HisfsTer26
ENST00000349258.8:c.785_795del	ENSP00000340650.4:p.Pro262HisfsTer26
NM_018676.3:c.785_795del	NP_061146.1:p.Pro262HisfsTer26
NM_199263.2:c.785_795del	NP_954872.1:p.Pro262HisfsTer26
NM_018676.4:c.785_795del MANE Select	NP_061146.1:p.Pro262HisfsTer26
NM_199263.3:c.785_795del	NP_954872.1:p.Pro262HisfsTer26