Canonical Allele Identifier: CA357618191

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903652T>G (hg19) ; chr4:g.87982500T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982500T>G , CM000666.2:g.87982500T>G	GRCh38
NC_000004.11:g.88903652T>G , CM000666.1:g.88903652T>G	GRCh37
NC_000004.10:g.89122676T>G	NCBI36
NG_030362.1:g.11851T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.426T>G	ENSP00000422973.2:p.Asp142Glu
ENST00000614857.5:c.549T>G	ENSP00000477824.2:p.Asp183Glu
ENST00000681973.1:n.776T>G
ENST00000682026.1:n.502T>G
ENST00000682448.1:n.2035T>G
ENST00000682554.1:n.1997T>G
ENST00000682599.1:n.3037T>G
ENST00000682627.1:n.469T>G
ENST00000682865.1:n.833T>G
ENST00000683087.1:n.563T>G
ENST00000683168.1:n.1303T>G
ENST00000683620.1:n.1731T>G
ENST00000684106.1:n.2799T>G
ENST00000684450.1:n.1608T>G
ENST00000684710.1:n.1840T>G
ENST00000395080.8:c.549T>G MANE Select	ENSP00000378517.3:p.Asp183Glu
ENST00000237623.11:c.507T>G	ENSP00000237623.7:p.Asp169Glu
ENST00000360804.4:c.468T>G	ENSP00000354042.4:p.Asp156Glu
ENST00000395080.7:c.549T>G	ENSP00000378517.3:p.Asp183Glu
ENST00000508233.5:c.426T>G	ENSP00000422973.1:p.Asp142Glu
ENST00000509659.5:n.838T>G
ENST00000614857.4:c.483T>G	ENSP00000477824.1:p.Asp161Glu
NM_000582.2:c.507T>G	NP_000573.1:p.Asp169Glu
NM_001040058.1:c.549T>G	NP_001035147.1:p.Asp183Glu
NM_001040060.1:c.468T>G	NP_001035149.1:p.Asp156Glu
NM_001251829.1:c.426T>G	NP_001238758.1:p.Asp142Glu
NM_001251830.1:c.588T>G	NP_001238759.1:p.Asp196Glu
NM_001040058.2:c.549T>G MANE Select	NP_001035147.1:p.Asp183Glu
NM_000582.3:c.507T>G	NP_000573.1:p.Asp169Glu
NM_001040060.2:c.468T>G	NP_001035149.1:p.Asp156Glu
NM_001251829.2:c.426T>G	NP_001238758.1:p.Asp142Glu
NM_001251830.2:c.588T>G	NP_001238759.1:p.Asp196Glu