Canonical Allele Identifier: CA357618232

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903663A>T (hg19) ; chr4:g.87982511A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982511A>T , CM000666.2:g.87982511A>T	GRCh38
NC_000004.11:g.88903663A>T , CM000666.1:g.88903663A>T	GRCh37
NC_000004.10:g.89122687A>T	NCBI36
NG_030362.1:g.11862A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.437A>T	ENSP00000422973.2:p.Glu146Val
ENST00000614857.5:c.560A>T	ENSP00000477824.2:p.Glu187Val
ENST00000681973.1:n.787A>T
ENST00000682026.1:n.513A>T
ENST00000682448.1:n.2046A>T
ENST00000682554.1:n.2008A>T
ENST00000682599.1:n.3048A>T
ENST00000682627.1:n.480A>T
ENST00000682865.1:n.844A>T
ENST00000683087.1:n.574A>T
ENST00000683168.1:n.1314A>T
ENST00000683620.1:n.1742A>T
ENST00000684106.1:n.2810A>T
ENST00000684450.1:n.1619A>T
ENST00000684710.1:n.1851A>T
ENST00000395080.8:c.560A>T MANE Select	ENSP00000378517.3:p.Glu187Val
ENST00000237623.11:c.518A>T	ENSP00000237623.7:p.Glu173Val
ENST00000360804.4:c.479A>T	ENSP00000354042.4:p.Glu160Val
ENST00000395080.7:c.560A>T	ENSP00000378517.3:p.Glu187Val
ENST00000508233.5:c.437A>T	ENSP00000422973.1:p.Glu146Val
ENST00000509659.5:n.849A>T
ENST00000614857.4:c.494A>T	ENSP00000477824.1:p.Glu165Val
NM_000582.2:c.518A>T	NP_000573.1:p.Glu173Val
NM_001040058.1:c.560A>T	NP_001035147.1:p.Glu187Val
NM_001040060.1:c.479A>T	NP_001035149.1:p.Glu160Val
NM_001251829.1:c.437A>T	NP_001238758.1:p.Glu146Val
NM_001251830.1:c.599A>T	NP_001238759.1:p.Glu200Val
NM_001040058.2:c.560A>T MANE Select	NP_001035147.1:p.Glu187Val
NM_000582.3:c.518A>T	NP_000573.1:p.Glu173Val
NM_001040060.2:c.479A>T	NP_001035149.1:p.Glu160Val
NM_001251829.2:c.437A>T	NP_001238758.1:p.Glu146Val
NM_001251830.2:c.599A>T	NP_001238759.1:p.Glu200Val