Canonical Allele Identifier: CA100858453

Gene: SPP1

Linked Data

• dbSNP Id: rs1126616
• MyVariant Identifiers: chr4:g.88903853C>G (hg19) ; chr4:g.87982701C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982701C>G , CM000666.2:g.87982701C>G	GRCh38
NC_000004.11:g.88903853C>G , CM000666.1:g.88903853C>G	GRCh37
NC_000004.10:g.89122877C>G	NCBI36
NG_030362.1:g.12052C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000508233.6:c.627C>G	ENSP00000422973.2:p.Ala209=
ENST00000614857.5:c.750C>G	ENSP00000477824.2:p.Ala250=
ENST00000681973.1:n.977C>G
ENST00000682026.1:n.703C>G
ENST00000682448.1:n.2236C>G
ENST00000682554.1:n.2198C>G
ENST00000682599.1:n.3238C>G
ENST00000682627.1:n.670C>G
ENST00000682865.1:n.1034C>G
ENST00000683087.1:n.764C>G
ENST00000683168.1:n.1504C>G
ENST00000683620.1:n.1932C>G
ENST00000684106.1:n.3000C>G
ENST00000684450.1:n.1809C>G
ENST00000684710.1:n.2041C>G
ENST00000395080.8:c.750C>G MANE Select	ENSP00000378517.3:p.Ala250=
ENST00000237623.11:c.708C>G	ENSP00000237623.7:p.Ala236=
ENST00000360804.4:c.669C>G	ENSP00000354042.4:p.Ala223=
ENST00000395080.7:c.750C>G	ENSP00000378517.3:p.Ala250=
ENST00000508233.5:c.627C>G	ENSP00000422973.1:p.Ala209=
ENST00000509659.5:n.1039C>G
ENST00000614857.4:c.684C>G	ENSP00000477824.1:p.Ala228=
NM_000582.2:c.708C>G	NP_000573.1:p.Ala236=
NM_001040058.1:c.750C>G	NP_001035147.1:p.Ala250=
NM_001040060.1:c.669C>G	NP_001035149.1:p.Ala223=
NM_001251829.1:c.627C>G	NP_001238758.1:p.Ala209=
NM_001251830.1:c.789C>G	NP_001238759.1:p.Ala263=
NM_001040058.2:c.750C>G MANE Select	NP_001035147.1:p.Ala250=
NM_000582.3:c.708C>G	NP_000573.1:p.Ala236=
NM_001040060.2:c.669C>G	NP_001035149.1:p.Ala223=
NM_001251829.2:c.627C>G	NP_001238758.1:p.Ala209=
NM_001251830.2:c.789C>G	NP_001238759.1:p.Ala263=