Canonical Allele Identifier: CA489673199

Gene: THBS1 FSIP1

Linked Data

• MyVariant Identifiers: chr15:g.39882080C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.39589879C>G , CM000677.2:g.39589879C>G	GRCh38
NC_000015.9:g.39882080C>G , CM000677.1:g.39882080C>G	GRCh37
NC_000015.8:g.37669372C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000260356.6:c.2001C>G (THBS1) MANE Select	ENSP00000260356.5:p.Gly667=
ENST00000642527.1:c.771-1305G>C (FSIP1)
ENST00000260356.5:c.2001C>G (THBS1)	ENSP00000260356.5:p.Gly667=
NM_003246.2:c.2001C>G (THBS1)	NP_003237.2:p.Gly667=
NM_003246.3:c.2001C>G (THBS1)	NP_003237.2:p.Gly667=
XM_011521970.1:c.2001C>G (THBS1)	XP_011520272.1:p.Gly667=
XM_011521971.1:c.1827C>G (THBS1)	XP_011520273.1:p.Gly609=
XR_931897.1:n.2176C>G (THBS1)
XM_011521971.2:c.1827C>G (THBS1)	XP_011520273.1:p.Gly609=
NM_003246.4:c.2001C>G (THBS1) MANE Select	NP_003237.2:p.Gly667=