Canonical Allele Identifier: CA2091759625

Gene: THSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.52397724C= , CM000675.2:g.52397724C=	GRCh38
NC_000013.10:g.52971859C= , CM000675.1:g.52971859C=	GRCh37
NC_000013.9:g.51869860C=	NCBI36
NG_047168.1:g.13771G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258613.5:c.529G= MANE Select	ENSP00000258613.4:p.Glu177=
ENST00000648254.1:c.529G=	ENSP00000497520.1:p.Glu177=
ENST00000258613.4:c.529G=	ENSP00000258613.4:p.Glu177=
ENST00000349258.8:c.529G=	ENSP00000340650.4:p.Glu177=
NM_018676.3:c.529G=	NP_061146.1:p.Glu177=
NM_199263.2:c.529G=	NP_954872.1:p.Glu177=
NM_018676.4:c.529G= MANE Select	NP_061146.1:p.Glu177=
NM_199263.3:c.529G=	NP_954872.1:p.Glu177=