Canonical Allele Identifier: CA1474551079

Gene: SPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982522T= , CM000666.2:g.87982522T=	GRCh38
NC_000004.11:g.88903674T= , CM000666.1:g.88903674T=	GRCh37
NC_000004.10:g.89122698T=	NCBI36
NG_030362.1:g.11873T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.448T=	ENSP00000422973.2:p.Ser150=
ENST00000614857.5:c.571T=	ENSP00000477824.2:p.Ser191=
ENST00000681973.1:n.798T=
ENST00000682026.1:n.524T=
ENST00000682448.1:n.2057T=
ENST00000682554.1:n.2019T=
ENST00000682599.1:n.3059T=
ENST00000682627.1:n.491T=
ENST00000682865.1:n.855T=
ENST00000683087.1:n.585T=
ENST00000683168.1:n.1325T=
ENST00000683620.1:n.1753T=
ENST00000684106.1:n.2821T=
ENST00000684450.1:n.1630T=
ENST00000684710.1:n.1862T=
ENST00000395080.8:c.571T= MANE Select	ENSP00000378517.3:p.Ser191=
ENST00000237623.11:c.529T=	ENSP00000237623.7:p.Ser177=
ENST00000360804.4:c.490T=	ENSP00000354042.4:p.Ser164=
ENST00000395080.7:c.571T=	ENSP00000378517.3:p.Ser191=
ENST00000508233.5:c.448T=	ENSP00000422973.1:p.Ser150=
ENST00000509659.5:n.860T=
ENST00000614857.4:c.505T=	ENSP00000477824.1:p.Ser169=
NM_000582.2:c.529T=	NP_000573.1:p.Ser177=
NM_001040058.1:c.571T=	NP_001035147.1:p.Ser191=
NM_001040060.1:c.490T=	NP_001035149.1:p.Ser164=
NM_001251829.1:c.448T=	NP_001238758.1:p.Ser150=
NM_001251830.1:c.610T=	NP_001238759.1:p.Ser204=
NM_001040058.2:c.571T= MANE Select	NP_001035147.1:p.Ser191=
NM_000582.3:c.529T=	NP_000573.1:p.Ser177=
NM_001040060.2:c.490T=	NP_001035149.1:p.Ser164=
NM_001251829.2:c.448T=	NP_001238758.1:p.Ser150=
NM_001251830.2:c.610T=	NP_001238759.1:p.Ser204=