Canonical Allele Identifier: CA357618247
Gene: SPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87982514A>G , CM000666.2:g.87982514A>G GRCh38
NC_000004.11:g.88903666A>G , CM000666.1:g.88903666A>G GRCh37
NC_000004.10:g.89122690A>G NCBI36
NG_030362.1:g.11865A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000508233.6:c.440A>G ENSP00000422973.2:p.Asp147Gly
ENST00000614857.5:c.563A>G ENSP00000477824.2:p.Asp188Gly
ENST00000681973.1:n.790A>G
ENST00000682026.1:n.516A>G
ENST00000682448.1:n.2049A>G
ENST00000682554.1:n.2011A>G
ENST00000682599.1:n.3051A>G
ENST00000682627.1:n.483A>G
ENST00000682865.1:n.847A>G
ENST00000683087.1:n.577A>G
ENST00000683168.1:n.1317A>G
ENST00000683620.1:n.1745A>G
ENST00000684106.1:n.2813A>G
ENST00000684450.1:n.1622A>G
ENST00000684710.1:n.1854A>G
ENST00000395080.8:c.563A>G MANE Select ENSP00000378517.3:p.Asp188Gly
ENST00000237623.11:c.521A>G ENSP00000237623.7:p.Asp174Gly
ENST00000360804.4:c.482A>G ENSP00000354042.4:p.Asp161Gly
ENST00000395080.7:c.563A>G ENSP00000378517.3:p.Asp188Gly
ENST00000508233.5:c.440A>G ENSP00000422973.1:p.Asp147Gly
ENST00000509659.5:n.852A>G
ENST00000614857.4:c.497A>G ENSP00000477824.1:p.Asp166Gly
NM_000582.2:c.521A>G NP_000573.1:p.Asp174Gly
NM_001040058.1:c.563A>G NP_001035147.1:p.Asp188Gly
NM_001040060.1:c.482A>G NP_001035149.1:p.Asp161Gly
NM_001251829.1:c.440A>G NP_001238758.1:p.Asp147Gly
NM_001251830.1:c.602A>G NP_001238759.1:p.Asp201Gly
NM_001040058.2:c.563A>G MANE Select NP_001035147.1:p.Asp188Gly
NM_000582.3:c.521A>G NP_000573.1:p.Asp174Gly
NM_001040060.2:c.482A>G NP_001035149.1:p.Asp161Gly
NM_001251829.2:c.440A>G NP_001238758.1:p.Asp147Gly
NM_001251830.2:c.602A>G NP_001238759.1:p.Asp201Gly