Canonical Allele Identifier: CA1474551075

Gene: SPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982513G= , CM000666.2:g.87982513G=	GRCh38
NC_000004.11:g.88903665G= , CM000666.1:g.88903665G=	GRCh37
NC_000004.10:g.89122689G=	NCBI36
NG_030362.1:g.11864G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.439G=	ENSP00000422973.2:p.Asp147=
ENST00000614857.5:c.562G=	ENSP00000477824.2:p.Asp188=
ENST00000681973.1:n.789G=
ENST00000682026.1:n.515G=
ENST00000682448.1:n.2048G=
ENST00000682554.1:n.2010G=
ENST00000682599.1:n.3050G=
ENST00000682627.1:n.482G=
ENST00000682865.1:n.846G=
ENST00000683087.1:n.576G=
ENST00000683168.1:n.1316G=
ENST00000683620.1:n.1744G=
ENST00000684106.1:n.2812G=
ENST00000684450.1:n.1621G=
ENST00000684710.1:n.1853G=
ENST00000395080.8:c.562G= MANE Select	ENSP00000378517.3:p.Asp188=
ENST00000237623.11:c.520G=	ENSP00000237623.7:p.Asp174=
ENST00000360804.4:c.481G=	ENSP00000354042.4:p.Asp161=
ENST00000395080.7:c.562G=	ENSP00000378517.3:p.Asp188=
ENST00000508233.5:c.439G=	ENSP00000422973.1:p.Asp147=
ENST00000509659.5:n.851G=
ENST00000614857.4:c.496G=	ENSP00000477824.1:p.Asp166=
NM_000582.2:c.520G=	NP_000573.1:p.Asp174=
NM_001040058.1:c.562G=	NP_001035147.1:p.Asp188=
NM_001040060.1:c.481G=	NP_001035149.1:p.Asp161=
NM_001251829.1:c.439G=	NP_001238758.1:p.Asp147=
NM_001251830.1:c.601G=	NP_001238759.1:p.Asp201=
NM_001040058.2:c.562G= MANE Select	NP_001035147.1:p.Asp188=
NM_000582.3:c.520G=	NP_000573.1:p.Asp174=
NM_001040060.2:c.481G=	NP_001035149.1:p.Asp161=
NM_001251829.2:c.439G=	NP_001238758.1:p.Asp147=
NM_001251830.2:c.601G=	NP_001238759.1:p.Asp201=