Canonical Allele Identifier: CA440296390

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903655T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982503T>G , CM000666.2:g.87982503T>G	GRCh38
NC_000004.11:g.88903655T>G , CM000666.1:g.88903655T>G	GRCh37
NC_000004.10:g.89122679T>G	NCBI36
NG_030362.1:g.11854T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.429T>G	ENSP00000422973.2:p.Ala143=
ENST00000614857.5:c.552T>G	ENSP00000477824.2:p.Ala184=
ENST00000681973.1:n.779T>G
ENST00000682026.1:n.505T>G
ENST00000682448.1:n.2038T>G
ENST00000682554.1:n.2000T>G
ENST00000682599.1:n.3040T>G
ENST00000682627.1:n.472T>G
ENST00000682865.1:n.836T>G
ENST00000683087.1:n.566T>G
ENST00000683168.1:n.1306T>G
ENST00000683620.1:n.1734T>G
ENST00000684106.1:n.2802T>G
ENST00000684450.1:n.1611T>G
ENST00000684710.1:n.1843T>G
ENST00000395080.8:c.552T>G MANE Select	ENSP00000378517.3:p.Ala184=
ENST00000237623.11:c.510T>G	ENSP00000237623.7:p.Ala170=
ENST00000360804.4:c.471T>G	ENSP00000354042.4:p.Ala157=
ENST00000395080.7:c.552T>G	ENSP00000378517.3:p.Ala184=
ENST00000508233.5:c.429T>G	ENSP00000422973.1:p.Ala143=
ENST00000509659.5:n.841T>G
ENST00000614857.4:c.486T>G	ENSP00000477824.1:p.Ala162=
NM_000582.2:c.510T>G	NP_000573.1:p.Ala170=
NM_001040058.1:c.552T>G	NP_001035147.1:p.Ala184=
NM_001040060.1:c.471T>G	NP_001035149.1:p.Ala157=
NM_001251829.1:c.429T>G	NP_001238758.1:p.Ala143=
NM_001251830.1:c.591T>G	NP_001238759.1:p.Ala197=
NM_001040058.2:c.552T>G MANE Select	NP_001035147.1:p.Ala184=
NM_000582.3:c.510T>G	NP_000573.1:p.Ala170=
NM_001040060.2:c.471T>G	NP_001035149.1:p.Ala157=
NM_001251829.2:c.429T>G	NP_001238758.1:p.Ala143=
NM_001251830.2:c.591T>G	NP_001238759.1:p.Ala197=