Canonical Allele Identifier: CA357618228
Gene: SPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87982510G>C , CM000666.2:g.87982510G>C GRCh38
NC_000004.11:g.88903662G>C , CM000666.1:g.88903662G>C GRCh37
NC_000004.10:g.89122686G>C NCBI36
NG_030362.1:g.11861G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000508233.6:c.436G>C ENSP00000422973.2:p.Glu146Gln
ENST00000614857.5:c.559G>C ENSP00000477824.2:p.Glu187Gln
ENST00000681973.1:n.786G>C
ENST00000682026.1:n.512G>C
ENST00000682448.1:n.2045G>C
ENST00000682554.1:n.2007G>C
ENST00000682599.1:n.3047G>C
ENST00000682627.1:n.479G>C
ENST00000682865.1:n.843G>C
ENST00000683087.1:n.573G>C
ENST00000683168.1:n.1313G>C
ENST00000683620.1:n.1741G>C
ENST00000684106.1:n.2809G>C
ENST00000684450.1:n.1618G>C
ENST00000684710.1:n.1850G>C
ENST00000395080.8:c.559G>C MANE Select ENSP00000378517.3:p.Glu187Gln
ENST00000237623.11:c.517G>C ENSP00000237623.7:p.Glu173Gln
ENST00000360804.4:c.478G>C ENSP00000354042.4:p.Glu160Gln
ENST00000395080.7:c.559G>C ENSP00000378517.3:p.Glu187Gln
ENST00000508233.5:c.436G>C ENSP00000422973.1:p.Glu146Gln
ENST00000509659.5:n.848G>C
ENST00000614857.4:c.493G>C ENSP00000477824.1:p.Glu165Gln
NM_000582.2:c.517G>C NP_000573.1:p.Glu173Gln
NM_001040058.1:c.559G>C NP_001035147.1:p.Glu187Gln
NM_001040060.1:c.478G>C NP_001035149.1:p.Glu160Gln
NM_001251829.1:c.436G>C NP_001238758.1:p.Glu146Gln
NM_001251830.1:c.598G>C NP_001238759.1:p.Glu200Gln
NM_001040058.2:c.559G>C MANE Select NP_001035147.1:p.Glu187Gln
NM_000582.3:c.517G>C NP_000573.1:p.Glu173Gln
NM_001040060.2:c.478G>C NP_001035149.1:p.Glu160Gln
NM_001251829.2:c.436G>C NP_001238758.1:p.Glu146Gln
NM_001251830.2:c.598G>C NP_001238759.1:p.Glu200Gln