Canonical Allele Identifier: CA357618220

Gene: SPP1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.434A>T	ENSP00000422973.2:p.Asp145Val
ENST00000614857.5:c.557A>T	ENSP00000477824.2:p.Asp186Val
ENST00000681973.1:n.784A>T
ENST00000682026.1:n.510A>T
ENST00000682448.1:n.2043A>T
ENST00000682554.1:n.2005A>T
ENST00000682599.1:n.3045A>T
ENST00000682627.1:n.477A>T
ENST00000682865.1:n.841A>T
ENST00000683087.1:n.571A>T
ENST00000683168.1:n.1311A>T
ENST00000683620.1:n.1739A>T
ENST00000684106.1:n.2807A>T
ENST00000684450.1:n.1616A>T
ENST00000684710.1:n.1848A>T
ENST00000395080.8:c.557A>T MANE Select	ENSP00000378517.3:p.Asp186Val
ENST00000237623.11:c.515A>T	ENSP00000237623.7:p.Asp172Val
ENST00000360804.4:c.476A>T	ENSP00000354042.4:p.Asp159Val
ENST00000395080.7:c.557A>T	ENSP00000378517.3:p.Asp186Val
ENST00000508233.5:c.434A>T	ENSP00000422973.1:p.Asp145Val
ENST00000509659.5:n.846A>T
ENST00000614857.4:c.491A>T	ENSP00000477824.1:p.Asp164Val
NM_000582.2:c.515A>T	NP_000573.1:p.Asp172Val
NM_001040058.1:c.557A>T	NP_001035147.1:p.Asp186Val
NM_001040060.1:c.476A>T	NP_001035149.1:p.Asp159Val
NM_001251829.1:c.434A>T	NP_001238758.1:p.Asp145Val
NM_001251830.1:c.596A>T	NP_001238759.1:p.Asp199Val
NM_001040058.2:c.557A>T MANE Select	NP_001035147.1:p.Asp186Val
NM_000582.3:c.515A>T	NP_000573.1:p.Asp172Val
NM_001040060.2:c.476A>T	NP_001035149.1:p.Asp159Val
NM_001251829.2:c.434A>T	NP_001238758.1:p.Asp145Val
NM_001251830.2:c.596A>T	NP_001238759.1:p.Asp199Val