Canonical Allele Identifier: CA357618222
Gene: SPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87982509C>A , CM000666.2:g.87982509C>A GRCh38
NC_000004.11:g.88903661C>A , CM000666.1:g.88903661C>A GRCh37
NC_000004.10:g.89122685C>A NCBI36
NG_030362.1:g.11860C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000508233.6:c.435C>A ENSP00000422973.2:p.Asp145Glu
ENST00000614857.5:c.558C>A ENSP00000477824.2:p.Asp186Glu
ENST00000681973.1:n.785C>A
ENST00000682026.1:n.511C>A
ENST00000682448.1:n.2044C>A
ENST00000682554.1:n.2006C>A
ENST00000682599.1:n.3046C>A
ENST00000682627.1:n.478C>A
ENST00000682865.1:n.842C>A
ENST00000683087.1:n.572C>A
ENST00000683168.1:n.1312C>A
ENST00000683620.1:n.1740C>A
ENST00000684106.1:n.2808C>A
ENST00000684450.1:n.1617C>A
ENST00000684710.1:n.1849C>A
ENST00000395080.8:c.558C>A MANE Select ENSP00000378517.3:p.Asp186Glu
ENST00000237623.11:c.516C>A ENSP00000237623.7:p.Asp172Glu
ENST00000360804.4:c.477C>A ENSP00000354042.4:p.Asp159Glu
ENST00000395080.7:c.558C>A ENSP00000378517.3:p.Asp186Glu
ENST00000508233.5:c.435C>A ENSP00000422973.1:p.Asp145Glu
ENST00000509659.5:n.847C>A
ENST00000614857.4:c.492C>A ENSP00000477824.1:p.Asp164Glu
NM_000582.2:c.516C>A NP_000573.1:p.Asp172Glu
NM_001040058.1:c.558C>A NP_001035147.1:p.Asp186Glu
NM_001040060.1:c.477C>A NP_001035149.1:p.Asp159Glu
NM_001251829.1:c.435C>A NP_001238758.1:p.Asp145Glu
NM_001251830.1:c.597C>A NP_001238759.1:p.Asp199Glu
NM_001040058.2:c.558C>A MANE Select NP_001035147.1:p.Asp186Glu
NM_000582.3:c.516C>A NP_000573.1:p.Asp172Glu
NM_001040060.2:c.477C>A NP_001035149.1:p.Asp159Glu
NM_001251829.2:c.435C>A NP_001238758.1:p.Asp145Glu
NM_001251830.2:c.597C>A NP_001238759.1:p.Asp199Glu