Canonical Allele Identifier: CA440296400

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903673C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982521C>G , CM000666.2:g.87982521C>G	GRCh38
NC_000004.11:g.88903673C>G , CM000666.1:g.88903673C>G	GRCh37
NC_000004.10:g.89122697C>G	NCBI36
NG_030362.1:g.11872C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.447C>G	ENSP00000422973.2:p.Thr149=
ENST00000614857.5:c.570C>G	ENSP00000477824.2:p.Thr190=
ENST00000681973.1:n.797C>G
ENST00000682026.1:n.523C>G
ENST00000682448.1:n.2056C>G
ENST00000682554.1:n.2018C>G
ENST00000682599.1:n.3058C>G
ENST00000682627.1:n.490C>G
ENST00000682865.1:n.854C>G
ENST00000683087.1:n.584C>G
ENST00000683168.1:n.1324C>G
ENST00000683620.1:n.1752C>G
ENST00000684106.1:n.2820C>G
ENST00000684450.1:n.1629C>G
ENST00000684710.1:n.1861C>G
ENST00000395080.8:c.570C>G MANE Select	ENSP00000378517.3:p.Thr190=
ENST00000237623.11:c.528C>G	ENSP00000237623.7:p.Thr176=
ENST00000360804.4:c.489C>G	ENSP00000354042.4:p.Thr163=
ENST00000395080.7:c.570C>G	ENSP00000378517.3:p.Thr190=
ENST00000508233.5:c.447C>G	ENSP00000422973.1:p.Thr149=
ENST00000509659.5:n.859C>G
ENST00000614857.4:c.504C>G	ENSP00000477824.1:p.Thr168=
NM_000582.2:c.528C>G	NP_000573.1:p.Thr176=
NM_001040058.1:c.570C>G	NP_001035147.1:p.Thr190=
NM_001040060.1:c.489C>G	NP_001035149.1:p.Thr163=
NM_001251829.1:c.447C>G	NP_001238758.1:p.Thr149=
NM_001251830.1:c.609C>G	NP_001238759.1:p.Thr203=
NM_001040058.2:c.570C>G MANE Select	NP_001035147.1:p.Thr190=
NM_000582.3:c.528C>G	NP_000573.1:p.Thr176=
NM_001040060.2:c.489C>G	NP_001035149.1:p.Thr163=
NM_001251829.2:c.447C>G	NP_001238758.1:p.Thr149=
NM_001251830.2:c.609C>G	NP_001238759.1:p.Thr203=