Canonical Allele Identifier: CA357618216

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903660A>C (hg19) ; chr4:g.87982508A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982508A>C , CM000666.2:g.87982508A>C	GRCh38
NC_000004.11:g.88903660A>C , CM000666.1:g.88903660A>C	GRCh37
NC_000004.10:g.89122684A>C	NCBI36
NG_030362.1:g.11859A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.434A>C	ENSP00000422973.2:p.Asp145Ala
ENST00000614857.5:c.557A>C	ENSP00000477824.2:p.Asp186Ala
ENST00000681973.1:n.784A>C
ENST00000682026.1:n.510A>C
ENST00000682448.1:n.2043A>C
ENST00000682554.1:n.2005A>C
ENST00000682599.1:n.3045A>C
ENST00000682627.1:n.477A>C
ENST00000682865.1:n.841A>C
ENST00000683087.1:n.571A>C
ENST00000683168.1:n.1311A>C
ENST00000683620.1:n.1739A>C
ENST00000684106.1:n.2807A>C
ENST00000684450.1:n.1616A>C
ENST00000684710.1:n.1848A>C
ENST00000395080.8:c.557A>C MANE Select	ENSP00000378517.3:p.Asp186Ala
ENST00000237623.11:c.515A>C	ENSP00000237623.7:p.Asp172Ala
ENST00000360804.4:c.476A>C	ENSP00000354042.4:p.Asp159Ala
ENST00000395080.7:c.557A>C	ENSP00000378517.3:p.Asp186Ala
ENST00000508233.5:c.434A>C	ENSP00000422973.1:p.Asp145Ala
ENST00000509659.5:n.846A>C
ENST00000614857.4:c.491A>C	ENSP00000477824.1:p.Asp164Ala
NM_000582.2:c.515A>C	NP_000573.1:p.Asp172Ala
NM_001040058.1:c.557A>C	NP_001035147.1:p.Asp186Ala
NM_001040060.1:c.476A>C	NP_001035149.1:p.Asp159Ala
NM_001251829.1:c.434A>C	NP_001238758.1:p.Asp145Ala
NM_001251830.1:c.596A>C	NP_001238759.1:p.Asp199Ala
NM_001040058.2:c.557A>C MANE Select	NP_001035147.1:p.Asp186Ala
NM_000582.3:c.515A>C	NP_000573.1:p.Asp172Ala
NM_001040060.2:c.476A>C	NP_001035149.1:p.Asp159Ala
NM_001251829.2:c.434A>C	NP_001238758.1:p.Asp145Ala
NM_001251830.2:c.596A>C	NP_001238759.1:p.Asp199Ala