Canonical Allele Identifier: CA1474550632

Gene: SPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87981540T= , CM000666.2:g.87981540T=	GRCh38
NC_000004.11:g.88902692T= , CM000666.1:g.88902692T=	GRCh37
NC_000004.10:g.89121716T=	NCBI36
NG_030362.1:g.10891T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.159T=	ENSP00000422973.2:p.Asp53=
ENST00000614857.5:c.282T=	ENSP00000477824.2:p.Asp94=
ENST00000681973.1:n.509T=
ENST00000682026.1:n.235T=
ENST00000682448.1:n.1768T=
ENST00000682554.1:n.1730T=
ENST00000682599.1:n.2770T=
ENST00000682627.1:n.202T=
ENST00000682655.1:c.282T=	ENSP00000508280.1:p.Asp94=
ENST00000682865.1:n.566T=
ENST00000683087.1:n.296T=
ENST00000683168.1:n.1036T=
ENST00000683620.1:n.1464T=
ENST00000684106.1:n.2532T=
ENST00000684450.1:n.1341T=
ENST00000684710.1:n.1573T=
ENST00000395080.8:c.282T= MANE Select	ENSP00000378517.3:p.Asp94=
ENST00000237623.11:c.240T=	ENSP00000237623.7:p.Asp80=
ENST00000360804.4:c.201T=	ENSP00000354042.4:p.Asp67=
ENST00000395080.7:c.282T=	ENSP00000378517.3:p.Asp94=
ENST00000508233.5:c.159T=	ENSP00000422973.1:p.Asp53=
ENST00000509334.5:n.539T=
ENST00000509659.5:n.571T=
ENST00000513981.5:n.581T=
ENST00000614857.4:c.277+5T=	ENSP00000477824.1:n.277+5T=
NM_000582.2:c.240T=	NP_000573.1:p.Asp80=
NM_001040058.1:c.282T=	NP_001035147.1:p.Asp94=
NM_001040060.1:c.201T=	NP_001035149.1:p.Asp67=
NM_001251829.1:c.159T=	NP_001238758.1:p.Asp53=
NM_001251830.1:c.321T=	NP_001238759.1:p.Asp107=
NM_001040058.2:c.282T= MANE Select	NP_001035147.1:p.Asp94=
NM_000582.3:c.240T=	NP_000573.1:p.Asp80=
NM_001040060.2:c.201T=	NP_001035149.1:p.Asp67=
NM_001251829.2:c.159T=	NP_001238758.1:p.Asp53=
NM_001251830.2:c.321T=	NP_001238759.1:p.Asp107=