Canonical Allele Identifier: CA1474551077

Gene: SPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982517T= , CM000666.2:g.87982517T=	GRCh38
NC_000004.11:g.88903669T= , CM000666.1:g.88903669T=	GRCh37
NC_000004.10:g.89122693T=	NCBI36
NG_030362.1:g.11868T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.443T=	ENSP00000422973.2:p.Ile148=
ENST00000614857.5:c.566T=	ENSP00000477824.2:p.Ile189=
ENST00000681973.1:n.793T=
ENST00000682026.1:n.519T=
ENST00000682448.1:n.2052T=
ENST00000682554.1:n.2014T=
ENST00000682599.1:n.3054T=
ENST00000682627.1:n.486T=
ENST00000682865.1:n.850T=
ENST00000683087.1:n.580T=
ENST00000683168.1:n.1320T=
ENST00000683620.1:n.1748T=
ENST00000684106.1:n.2816T=
ENST00000684450.1:n.1625T=
ENST00000684710.1:n.1857T=
ENST00000395080.8:c.566T= MANE Select	ENSP00000378517.3:p.Ile189=
ENST00000237623.11:c.524T=	ENSP00000237623.7:p.Ile175=
ENST00000360804.4:c.485T=	ENSP00000354042.4:p.Ile162=
ENST00000395080.7:c.566T=	ENSP00000378517.3:p.Ile189=
ENST00000508233.5:c.443T=	ENSP00000422973.1:p.Ile148=
ENST00000509659.5:n.855T=
ENST00000614857.4:c.500T=	ENSP00000477824.1:p.Ile167=
NM_000582.2:c.524T=	NP_000573.1:p.Ile175=
NM_001040058.1:c.566T=	NP_001035147.1:p.Ile189=
NM_001040060.1:c.485T=	NP_001035149.1:p.Ile162=
NM_001251829.1:c.443T=	NP_001238758.1:p.Ile148=
NM_001251830.1:c.605T=	NP_001238759.1:p.Ile202=
NM_001040058.2:c.566T= MANE Select	NP_001035147.1:p.Ile189=
NM_000582.3:c.524T=	NP_000573.1:p.Ile175=
NM_001040060.2:c.485T=	NP_001035149.1:p.Ile162=
NM_001251829.2:c.443T=	NP_001238758.1:p.Ile148=
NM_001251830.2:c.605T=	NP_001238759.1:p.Ile202=