Canonical Allele Identifier: CA1474551069

Gene: SPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982498G= , CM000666.2:g.87982498G=	GRCh38
NC_000004.11:g.88903650G= , CM000666.1:g.88903650G=	GRCh37
NC_000004.10:g.89122674G=	NCBI36
NG_030362.1:g.11849G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.424G=	ENSP00000422973.2:p.Asp142=
ENST00000614857.5:c.547G=	ENSP00000477824.2:p.Asp183=
ENST00000681973.1:n.774G=
ENST00000682026.1:n.500G=
ENST00000682448.1:n.2033G=
ENST00000682554.1:n.1995G=
ENST00000682599.1:n.3035G=
ENST00000682627.1:n.467G=
ENST00000682865.1:n.831G=
ENST00000683087.1:n.561G=
ENST00000683168.1:n.1301G=
ENST00000683620.1:n.1729G=
ENST00000684106.1:n.2797G=
ENST00000684450.1:n.1606G=
ENST00000684710.1:n.1838G=
ENST00000395080.8:c.547G= MANE Select	ENSP00000378517.3:p.Asp183=
ENST00000237623.11:c.505G=	ENSP00000237623.7:p.Asp169=
ENST00000360804.4:c.466G=	ENSP00000354042.4:p.Asp156=
ENST00000395080.7:c.547G=	ENSP00000378517.3:p.Asp183=
ENST00000508233.5:c.424G=	ENSP00000422973.1:p.Asp142=
ENST00000509659.5:n.836G=
ENST00000614857.4:c.481G=	ENSP00000477824.1:p.Asp161=
NM_000582.2:c.505G=	NP_000573.1:p.Asp169=
NM_001040058.1:c.547G=	NP_001035147.1:p.Asp183=
NM_001040060.1:c.466G=	NP_001035149.1:p.Asp156=
NM_001251829.1:c.424G=	NP_001238758.1:p.Asp142=
NM_001251830.1:c.586G=	NP_001238759.1:p.Asp196=
NM_001040058.2:c.547G= MANE Select	NP_001035147.1:p.Asp183=
NM_000582.3:c.505G=	NP_000573.1:p.Asp169=
NM_001040060.2:c.466G=	NP_001035149.1:p.Asp156=
NM_001251829.2:c.424G=	NP_001238758.1:p.Asp142=
NM_001251830.2:c.586G=	NP_001238759.1:p.Asp196=