Canonical Allele Identifier: CA357618279

Gene: SPP1

Linked Data

• dbSNP Id: rs1725689074
• MyVariant Identifiers: chr4:g.88903674T>G (hg19) ; chr4:g.87982522T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982522T>G , CM000666.2:g.87982522T>G	GRCh38
NC_000004.11:g.88903674T>G , CM000666.1:g.88903674T>G	GRCh37
NC_000004.10:g.89122698T>G	NCBI36
NG_030362.1:g.11873T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.448T>G	ENSP00000422973.2:p.Ser150Ala
ENST00000614857.5:c.571T>G	ENSP00000477824.2:p.Ser191Ala
ENST00000681973.1:n.798T>G
ENST00000682026.1:n.524T>G
ENST00000682448.1:n.2057T>G
ENST00000682554.1:n.2019T>G
ENST00000682599.1:n.3059T>G
ENST00000682627.1:n.491T>G
ENST00000682865.1:n.855T>G
ENST00000683087.1:n.585T>G
ENST00000683168.1:n.1325T>G
ENST00000683620.1:n.1753T>G
ENST00000684106.1:n.2821T>G
ENST00000684450.1:n.1630T>G
ENST00000684710.1:n.1862T>G
ENST00000395080.8:c.571T>G MANE Select	ENSP00000378517.3:p.Ser191Ala
ENST00000237623.11:c.529T>G	ENSP00000237623.7:p.Ser177Ala
ENST00000360804.4:c.490T>G	ENSP00000354042.4:p.Ser164Ala
ENST00000395080.7:c.571T>G	ENSP00000378517.3:p.Ser191Ala
ENST00000508233.5:c.448T>G	ENSP00000422973.1:p.Ser150Ala
ENST00000509659.5:n.860T>G
ENST00000614857.4:c.505T>G	ENSP00000477824.1:p.Ser169Ala
NM_000582.2:c.529T>G	NP_000573.1:p.Ser177Ala
NM_001040058.1:c.571T>G	NP_001035147.1:p.Ser191Ala
NM_001040060.1:c.490T>G	NP_001035149.1:p.Ser164Ala
NM_001251829.1:c.448T>G	NP_001238758.1:p.Ser150Ala
NM_001251830.1:c.610T>G	NP_001238759.1:p.Ser204Ala
NM_001040058.2:c.571T>G MANE Select	NP_001035147.1:p.Ser191Ala
NM_000582.3:c.529T>G	NP_000573.1:p.Ser177Ala
NM_001040060.2:c.490T>G	NP_001035149.1:p.Ser164Ala
NM_001251829.2:c.448T>G	NP_001238758.1:p.Ser150Ala
NM_001251830.2:c.610T>G	NP_001238759.1:p.Ser204Ala