Canonical Allele Identifier: CA1474551073

Gene: SPP1

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.436G=	ENSP00000422973.2:p.Glu146=
ENST00000614857.5:c.559G=	ENSP00000477824.2:p.Glu187=
ENST00000681973.1:n.786G=
ENST00000682026.1:n.512G=
ENST00000682448.1:n.2045G=
ENST00000682554.1:n.2007G=
ENST00000682599.1:n.3047G=
ENST00000682627.1:n.479G=
ENST00000682865.1:n.843G=
ENST00000683087.1:n.573G=
ENST00000683168.1:n.1313G=
ENST00000683620.1:n.1741G=
ENST00000684106.1:n.2809G=
ENST00000684450.1:n.1618G=
ENST00000684710.1:n.1850G=
ENST00000395080.8:c.559G= MANE Select	ENSP00000378517.3:p.Glu187=
ENST00000237623.11:c.517G=	ENSP00000237623.7:p.Glu173=
ENST00000360804.4:c.478G=	ENSP00000354042.4:p.Glu160=
ENST00000395080.7:c.559G=	ENSP00000378517.3:p.Glu187=
ENST00000508233.5:c.436G=	ENSP00000422973.1:p.Glu146=
ENST00000509659.5:n.848G=
ENST00000614857.4:c.493G=	ENSP00000477824.1:p.Glu165=
NM_000582.2:c.517G=	NP_000573.1:p.Glu173=
NM_001040058.1:c.559G=	NP_001035147.1:p.Glu187=
NM_001040060.1:c.478G=	NP_001035149.1:p.Glu160=
NM_001251829.1:c.436G=	NP_001238758.1:p.Glu146=
NM_001251830.1:c.598G=	NP_001238759.1:p.Glu200=
NM_001040058.2:c.559G= MANE Select	NP_001035147.1:p.Glu187=
NM_000582.3:c.517G=	NP_000573.1:p.Glu173=
NM_001040060.2:c.478G=	NP_001035149.1:p.Glu160=
NM_001251829.2:c.436G=	NP_001238758.1:p.Glu146=
NM_001251830.2:c.598G=	NP_001238759.1:p.Glu200=