Canonical Allele Identifier: CA357618183

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903651A>T (hg19) ; chr4:g.87982499A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982499A>T , CM000666.2:g.87982499A>T	GRCh38
NC_000004.11:g.88903651A>T , CM000666.1:g.88903651A>T	GRCh37
NC_000004.10:g.89122675A>T	NCBI36
NG_030362.1:g.11850A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.425A>T	ENSP00000422973.2:p.Asp142Val
ENST00000614857.5:c.548A>T	ENSP00000477824.2:p.Asp183Val
ENST00000681973.1:n.775A>T
ENST00000682026.1:n.501A>T
ENST00000682448.1:n.2034A>T
ENST00000682554.1:n.1996A>T
ENST00000682599.1:n.3036A>T
ENST00000682627.1:n.468A>T
ENST00000682865.1:n.832A>T
ENST00000683087.1:n.562A>T
ENST00000683168.1:n.1302A>T
ENST00000683620.1:n.1730A>T
ENST00000684106.1:n.2798A>T
ENST00000684450.1:n.1607A>T
ENST00000684710.1:n.1839A>T
ENST00000395080.8:c.548A>T MANE Select	ENSP00000378517.3:p.Asp183Val
ENST00000237623.11:c.506A>T	ENSP00000237623.7:p.Asp169Val
ENST00000360804.4:c.467A>T	ENSP00000354042.4:p.Asp156Val
ENST00000395080.7:c.548A>T	ENSP00000378517.3:p.Asp183Val
ENST00000508233.5:c.425A>T	ENSP00000422973.1:p.Asp142Val
ENST00000509659.5:n.837A>T
ENST00000614857.4:c.482A>T	ENSP00000477824.1:p.Asp161Val
NM_000582.2:c.506A>T	NP_000573.1:p.Asp169Val
NM_001040058.1:c.548A>T	NP_001035147.1:p.Asp183Val
NM_001040060.1:c.467A>T	NP_001035149.1:p.Asp156Val
NM_001251829.1:c.425A>T	NP_001238758.1:p.Asp142Val
NM_001251830.1:c.587A>T	NP_001238759.1:p.Asp196Val
NM_001040058.2:c.548A>T MANE Select	NP_001035147.1:p.Asp183Val
NM_000582.3:c.506A>T	NP_000573.1:p.Asp169Val
NM_001040060.2:c.467A>T	NP_001035149.1:p.Asp156Val
NM_001251829.2:c.425A>T	NP_001238758.1:p.Asp142Val
NM_001251830.2:c.587A>T	NP_001238759.1:p.Asp196Val