Canonical Allele Identifier: CA357618198

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903654C>G (hg19) ; chr4:g.87982502C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982502C>G , CM000666.2:g.87982502C>G	GRCh38
NC_000004.11:g.88903654C>G , CM000666.1:g.88903654C>G	GRCh37
NC_000004.10:g.89122678C>G	NCBI36
NG_030362.1:g.11853C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.428C>G	ENSP00000422973.2:p.Ala143Gly
ENST00000614857.5:c.551C>G	ENSP00000477824.2:p.Ala184Gly
ENST00000681973.1:n.778C>G
ENST00000682026.1:n.504C>G
ENST00000682448.1:n.2037C>G
ENST00000682554.1:n.1999C>G
ENST00000682599.1:n.3039C>G
ENST00000682627.1:n.471C>G
ENST00000682865.1:n.835C>G
ENST00000683087.1:n.565C>G
ENST00000683168.1:n.1305C>G
ENST00000683620.1:n.1733C>G
ENST00000684106.1:n.2801C>G
ENST00000684450.1:n.1610C>G
ENST00000684710.1:n.1842C>G
ENST00000395080.8:c.551C>G MANE Select	ENSP00000378517.3:p.Ala184Gly
ENST00000237623.11:c.509C>G	ENSP00000237623.7:p.Ala170Gly
ENST00000360804.4:c.470C>G	ENSP00000354042.4:p.Ala157Gly
ENST00000395080.7:c.551C>G	ENSP00000378517.3:p.Ala184Gly
ENST00000508233.5:c.428C>G	ENSP00000422973.1:p.Ala143Gly
ENST00000509659.5:n.840C>G
ENST00000614857.4:c.485C>G	ENSP00000477824.1:p.Ala162Gly
NM_000582.2:c.509C>G	NP_000573.1:p.Ala170Gly
NM_001040058.1:c.551C>G	NP_001035147.1:p.Ala184Gly
NM_001040060.1:c.470C>G	NP_001035149.1:p.Ala157Gly
NM_001251829.1:c.428C>G	NP_001238758.1:p.Ala143Gly
NM_001251830.1:c.590C>G	NP_001238759.1:p.Ala197Gly
NM_001040058.2:c.551C>G MANE Select	NP_001035147.1:p.Ala184Gly
NM_000582.3:c.509C>G	NP_000573.1:p.Ala170Gly
NM_001040060.2:c.470C>G	NP_001035149.1:p.Ala157Gly
NM_001251829.2:c.428C>G	NP_001238758.1:p.Ala143Gly
NM_001251830.2:c.590C>G	NP_001238759.1:p.Ala197Gly