Canonical Allele Identifier: CA2091759805

Gene: THSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.52397848_52397851delinsATTC , CM000675.2:g.52397848_52397851delinsATTC	GRCh38
NC_000013.10:g.52971983_52971986delinsATTC , CM000675.1:g.52971983_52971986delinsATTC	GRCh37
NC_000013.9:g.51869984_51869987delinsATTC	NCBI36
NG_047168.1:g.13644_13647delinsGAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258613.5:c.402_405delinsGAAT MANE Select	ENSP00000258613.4:p.Leu134=
ENST00000648254.1:c.402_405delinsGAAT	ENSP00000497520.1:p.Leu134=
ENST00000258613.4:c.402_405delinsGAAT	ENSP00000258613.4:p.Leu134=
ENST00000349258.8:c.402_405delinsGAAT	ENSP00000340650.4:p.Leu134=
NM_018676.3:c.402_405delinsGAAT	NP_061146.1:p.Leu134=
NM_199263.2:c.402_405delinsGAAT	NP_954872.1:p.Leu134=
NM_018676.4:c.402_405delinsGAAT MANE Select	NP_061146.1:p.Leu134=
NM_199263.3:c.402_405delinsGAAT	NP_954872.1:p.Leu134=