Canonical Allele Identifier: CA1474551067

Gene: SPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982495C= , CM000666.2:g.87982495C=	GRCh38
NC_000004.11:g.88903647C= , CM000666.1:g.88903647C=	GRCh37
NC_000004.10:g.89122671C=	NCBI36
NG_030362.1:g.11846C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.421C=	ENSP00000422973.2:p.Pro141=
ENST00000614857.5:c.544C=	ENSP00000477824.2:p.Pro182=
ENST00000681973.1:n.771C=
ENST00000682026.1:n.497C=
ENST00000682448.1:n.2030C=
ENST00000682554.1:n.1992C=
ENST00000682599.1:n.3032C=
ENST00000682627.1:n.464C=
ENST00000682865.1:n.828C=
ENST00000683087.1:n.558C=
ENST00000683168.1:n.1298C=
ENST00000683620.1:n.1726C=
ENST00000684106.1:n.2794C=
ENST00000684450.1:n.1603C=
ENST00000684710.1:n.1835C=
ENST00000395080.8:c.544C= MANE Select	ENSP00000378517.3:p.Pro182=
ENST00000237623.11:c.502C=	ENSP00000237623.7:p.Pro168=
ENST00000360804.4:c.463C=	ENSP00000354042.4:p.Pro155=
ENST00000395080.7:c.544C=	ENSP00000378517.3:p.Pro182=
ENST00000508233.5:c.421C=	ENSP00000422973.1:p.Pro141=
ENST00000509659.5:n.833C=
ENST00000614857.4:c.478C=	ENSP00000477824.1:p.Pro160=
NM_000582.2:c.502C=	NP_000573.1:p.Pro168=
NM_001040058.1:c.544C=	NP_001035147.1:p.Pro182=
NM_001040060.1:c.463C=	NP_001035149.1:p.Pro155=
NM_001251829.1:c.421C=	NP_001238758.1:p.Pro141=
NM_001251830.1:c.583C=	NP_001238759.1:p.Pro195=
NM_001040058.2:c.544C= MANE Select	NP_001035147.1:p.Pro182=
NM_000582.3:c.502C=	NP_000573.1:p.Pro168=
NM_001040060.2:c.463C=	NP_001035149.1:p.Pro155=
NM_001251829.2:c.421C=	NP_001238758.1:p.Pro141=
NM_001251830.2:c.583C=	NP_001238759.1:p.Pro195=