Canonical Allele Identifier: CA2171396569

Gene: THBS1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.39581269G= , CM000677.2:g.39581269G=	GRCh38
NC_000015.9:g.39873470G= , CM000677.1:g.39873470G=	GRCh37
NC_000015.8:g.37660762G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260356.6:c.-30+41G= MANE Select	ENSP00000260356.5:n.-30+41G=
ENST00000260356.5:c.-30+41G=	ENSP00000260356.5:n.-30+41G=
ENST00000397591.2:c.-151+41G=	ENSP00000380720.2:n.-151+41G=
NM_003246.2:c.-30+41G=	NP_003237.2:n.-30+41G=
NM_003246.3:c.-30+41G=	NP_003237.2:n.-30+41G=
XM_011521970.1:c.-151+41G=	XP_011520272.1:n.-151+41G=
XM_011521971.1:c.-30+41G=	XP_011520273.1:n.-30+41G=
XR_931897.1:n.146+41G=
XM_011521971.2:c.-30+41G=	XP_011520273.1:n.-30+41G=
NM_003246.4:c.-30+41G= MANE Select	NP_003237.2:n.-30+41G=