Canonical Allele Identifier: CA2091759528

Gene: THSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.52397624C= , CM000675.2:g.52397624C=	GRCh38
NC_000013.10:g.52971759C= , CM000675.1:g.52971759C=	GRCh37
NC_000013.9:g.51869760C=	NCBI36
NG_047168.1:g.13871G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258613.5:c.629G= MANE Select	ENSP00000258613.4:p.Gly210=
ENST00000648254.1:c.629G=	ENSP00000497520.1:p.Gly210=
ENST00000258613.4:c.629G=	ENSP00000258613.4:p.Gly210=
ENST00000349258.8:c.629G=	ENSP00000340650.4:p.Gly210=
NM_018676.3:c.629G=	NP_061146.1:p.Gly210=
NM_199263.2:c.629G=	NP_954872.1:p.Gly210=
NM_018676.4:c.629G= MANE Select	NP_061146.1:p.Gly210=
NM_199263.3:c.629G=	NP_954872.1:p.Gly210=