Canonical Allele Identifier: CA1474551076

Gene: SPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982515C= , CM000666.2:g.87982515C=	GRCh38
NC_000004.11:g.88903667C= , CM000666.1:g.88903667C=	GRCh37
NC_000004.10:g.89122691C=	NCBI36
NG_030362.1:g.11866C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.441C=	ENSP00000422973.2:p.Asp147=
ENST00000614857.5:c.564C=	ENSP00000477824.2:p.Asp188=
ENST00000681973.1:n.791C=
ENST00000682026.1:n.517C=
ENST00000682448.1:n.2050C=
ENST00000682554.1:n.2012C=
ENST00000682599.1:n.3052C=
ENST00000682627.1:n.484C=
ENST00000682865.1:n.848C=
ENST00000683087.1:n.578C=
ENST00000683168.1:n.1318C=
ENST00000683620.1:n.1746C=
ENST00000684106.1:n.2814C=
ENST00000684450.1:n.1623C=
ENST00000684710.1:n.1855C=
ENST00000395080.8:c.564C= MANE Select	ENSP00000378517.3:p.Asp188=
ENST00000237623.11:c.522C=	ENSP00000237623.7:p.Asp174=
ENST00000360804.4:c.483C=	ENSP00000354042.4:p.Asp161=
ENST00000395080.7:c.564C=	ENSP00000378517.3:p.Asp188=
ENST00000508233.5:c.441C=	ENSP00000422973.1:p.Asp147=
ENST00000509659.5:n.853C=
ENST00000614857.4:c.498C=	ENSP00000477824.1:p.Asp166=
NM_000582.2:c.522C=	NP_000573.1:p.Asp174=
NM_001040058.1:c.564C=	NP_001035147.1:p.Asp188=
NM_001040060.1:c.483C=	NP_001035149.1:p.Asp161=
NM_001251829.1:c.441C=	NP_001238758.1:p.Asp147=
NM_001251830.1:c.603C=	NP_001238759.1:p.Asp201=
NM_001040058.2:c.564C= MANE Select	NP_001035147.1:p.Asp188=
NM_000582.3:c.522C=	NP_000573.1:p.Asp174=
NM_001040060.2:c.483C=	NP_001035149.1:p.Asp161=
NM_001251829.2:c.441C=	NP_001238758.1:p.Asp147=
NM_001251830.2:c.603C=	NP_001238759.1:p.Asp201=