Canonical Allele Identifier: CA357618236
Gene: SPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87982511A>C , CM000666.2:g.87982511A>C GRCh38
NC_000004.11:g.88903663A>C , CM000666.1:g.88903663A>C GRCh37
NC_000004.10:g.89122687A>C NCBI36
NG_030362.1:g.11862A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000508233.6:c.437A>C ENSP00000422973.2:p.Glu146Ala
ENST00000614857.5:c.560A>C ENSP00000477824.2:p.Glu187Ala
ENST00000681973.1:n.787A>C
ENST00000682026.1:n.513A>C
ENST00000682448.1:n.2046A>C
ENST00000682554.1:n.2008A>C
ENST00000682599.1:n.3048A>C
ENST00000682627.1:n.480A>C
ENST00000682865.1:n.844A>C
ENST00000683087.1:n.574A>C
ENST00000683168.1:n.1314A>C
ENST00000683620.1:n.1742A>C
ENST00000684106.1:n.2810A>C
ENST00000684450.1:n.1619A>C
ENST00000684710.1:n.1851A>C
ENST00000395080.8:c.560A>C MANE Select ENSP00000378517.3:p.Glu187Ala
ENST00000237623.11:c.518A>C ENSP00000237623.7:p.Glu173Ala
ENST00000360804.4:c.479A>C ENSP00000354042.4:p.Glu160Ala
ENST00000395080.7:c.560A>C ENSP00000378517.3:p.Glu187Ala
ENST00000508233.5:c.437A>C ENSP00000422973.1:p.Glu146Ala
ENST00000509659.5:n.849A>C
ENST00000614857.4:c.494A>C ENSP00000477824.1:p.Glu165Ala
NM_000582.2:c.518A>C NP_000573.1:p.Glu173Ala
NM_001040058.1:c.560A>C NP_001035147.1:p.Glu187Ala
NM_001040060.1:c.479A>C NP_001035149.1:p.Glu160Ala
NM_001251829.1:c.437A>C NP_001238758.1:p.Glu146Ala
NM_001251830.1:c.599A>C NP_001238759.1:p.Glu200Ala
NM_001040058.2:c.560A>C MANE Select NP_001035147.1:p.Glu187Ala
NM_000582.3:c.518A>C NP_000573.1:p.Glu173Ala
NM_001040060.2:c.479A>C NP_001035149.1:p.Glu160Ala
NM_001251829.2:c.437A>C NP_001238758.1:p.Glu146Ala
NM_001251830.2:c.599A>C NP_001238759.1:p.Glu200Ala