Canonical Allele Identifier: CA2091759333

Gene: THSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.52397457_52397468delinsTGCATGGTGGAG , CM000675.2:g.52397457_52397468delinsTGCATGGTGGAG	GRCh38
NC_000013.10:g.52971592_52971603delinsTGCATGGTGGAG , CM000675.1:g.52971592_52971603delinsTGCATGGTGGAG	GRCh37
NC_000013.9:g.51869593_51869604delinsTGCATGGTGGAG	NCBI36
NG_047168.1:g.14027_14038delinsCTCCACCATGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258613.5:c.785_796delinsCTCCACCATGCA MANE Select	ENSP00000258613.4:p.Pro262=
ENST00000648254.1:c.785_796delinsCTCCACCATGCA	ENSP00000497520.1:p.Pro262=
ENST00000258613.4:c.785_796delinsCTCCACCATGCA	ENSP00000258613.4:p.Pro262=
ENST00000349258.8:c.785_796delinsCTCCACCATGCA	ENSP00000340650.4:p.Pro262=
NM_018676.3:c.785_796delinsCTCCACCATGCA	NP_061146.1:p.Pro262=
NM_199263.2:c.785_796delinsCTCCACCATGCA	NP_954872.1:p.Pro262=
NM_018676.4:c.785_796delinsCTCCACCATGCA MANE Select	NP_061146.1:p.Pro262=
NM_199263.3:c.785_796delinsCTCCACCATGCA	NP_954872.1:p.Pro262=