Canonical Allele Identifier: CA2091759387

Gene: THSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.52397501G= , CM000675.2:g.52397501G=	GRCh38
NC_000013.10:g.52971636G= , CM000675.1:g.52971636G=	GRCh37
NC_000013.9:g.51869637G=	NCBI36
NG_047168.1:g.13994C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258613.5:c.752C= MANE Select	ENSP00000258613.4:p.Thr251=
ENST00000648254.1:c.752C=	ENSP00000497520.1:p.Thr251=
ENST00000258613.4:c.752C=	ENSP00000258613.4:p.Thr251=
ENST00000349258.8:c.752C=	ENSP00000340650.4:p.Thr251=
NM_018676.3:c.752C=	NP_061146.1:p.Thr251=
NM_199263.2:c.752C=	NP_954872.1:p.Thr251=
NM_018676.4:c.752C= MANE Select	NP_061146.1:p.Thr251=
NM_199263.3:c.752C=	NP_954872.1:p.Thr251=