Canonical Allele Identifier: CA1474551071

Gene: SPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982503T= , CM000666.2:g.87982503T=	GRCh38
NC_000004.11:g.88903655T= , CM000666.1:g.88903655T=	GRCh37
NC_000004.10:g.89122679T=	NCBI36
NG_030362.1:g.11854T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.429T=	ENSP00000422973.2:p.Ala143=
ENST00000614857.5:c.552T=	ENSP00000477824.2:p.Ala184=
ENST00000681973.1:n.779T=
ENST00000682026.1:n.505T=
ENST00000682448.1:n.2038T=
ENST00000682554.1:n.2000T=
ENST00000682599.1:n.3040T=
ENST00000682627.1:n.472T=
ENST00000682865.1:n.836T=
ENST00000683087.1:n.566T=
ENST00000683168.1:n.1306T=
ENST00000683620.1:n.1734T=
ENST00000684106.1:n.2802T=
ENST00000684450.1:n.1611T=
ENST00000684710.1:n.1843T=
ENST00000395080.8:c.552T= MANE Select	ENSP00000378517.3:p.Ala184=
ENST00000237623.11:c.510T=	ENSP00000237623.7:p.Ala170=
ENST00000360804.4:c.471T=	ENSP00000354042.4:p.Ala157=
ENST00000395080.7:c.552T=	ENSP00000378517.3:p.Ala184=
ENST00000508233.5:c.429T=	ENSP00000422973.1:p.Ala143=
ENST00000509659.5:n.841T=
ENST00000614857.4:c.486T=	ENSP00000477824.1:p.Ala162=
NM_000582.2:c.510T=	NP_000573.1:p.Ala170=
NM_001040058.1:c.552T=	NP_001035147.1:p.Ala184=
NM_001040060.1:c.471T=	NP_001035149.1:p.Ala157=
NM_001251829.1:c.429T=	NP_001238758.1:p.Ala143=
NM_001251830.1:c.591T=	NP_001238759.1:p.Ala197=
NM_001040058.2:c.552T= MANE Select	NP_001035147.1:p.Ala184=
NM_000582.3:c.510T=	NP_000573.1:p.Ala170=
NM_001040060.2:c.471T=	NP_001035149.1:p.Ala157=
NM_001251829.2:c.429T=	NP_001238758.1:p.Ala143=
NM_001251830.2:c.591T=	NP_001238759.1:p.Ala197=