Canonical Allele Identifier: CA1474551078

Gene: SPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982520C= , CM000666.2:g.87982520C=	GRCh38
NC_000004.11:g.88903672C= , CM000666.1:g.88903672C=	GRCh37
NC_000004.10:g.89122696C=	NCBI36
NG_030362.1:g.11871C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.446C=	ENSP00000422973.2:p.Thr149=
ENST00000614857.5:c.569C=	ENSP00000477824.2:p.Thr190=
ENST00000681973.1:n.796C=
ENST00000682026.1:n.522C=
ENST00000682448.1:n.2055C=
ENST00000682554.1:n.2017C=
ENST00000682599.1:n.3057C=
ENST00000682627.1:n.489C=
ENST00000682865.1:n.853C=
ENST00000683087.1:n.583C=
ENST00000683168.1:n.1323C=
ENST00000683620.1:n.1751C=
ENST00000684106.1:n.2819C=
ENST00000684450.1:n.1628C=
ENST00000684710.1:n.1860C=
ENST00000395080.8:c.569C= MANE Select	ENSP00000378517.3:p.Thr190=
ENST00000237623.11:c.527C=	ENSP00000237623.7:p.Thr176=
ENST00000360804.4:c.488C=	ENSP00000354042.4:p.Thr163=
ENST00000395080.7:c.569C=	ENSP00000378517.3:p.Thr190=
ENST00000508233.5:c.446C=	ENSP00000422973.1:p.Thr149=
ENST00000509659.5:n.858C=
ENST00000614857.4:c.503C=	ENSP00000477824.1:p.Thr168=
NM_000582.2:c.527C=	NP_000573.1:p.Thr176=
NM_001040058.1:c.569C=	NP_001035147.1:p.Thr190=
NM_001040060.1:c.488C=	NP_001035149.1:p.Thr163=
NM_001251829.1:c.446C=	NP_001238758.1:p.Thr149=
NM_001251830.1:c.608C=	NP_001238759.1:p.Thr203=
NM_001040058.2:c.569C= MANE Select	NP_001035147.1:p.Thr190=
NM_000582.3:c.527C=	NP_000573.1:p.Thr176=
NM_001040060.2:c.488C=	NP_001035149.1:p.Thr163=
NM_001251829.2:c.446C=	NP_001238758.1:p.Thr149=
NM_001251830.2:c.608C=	NP_001238759.1:p.Thr203=