Canonical Allele Identifier: CA357618166

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903646C>G (hg19) ; chr4:g.87982494C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982494C>G , CM000666.2:g.87982494C>G	GRCh38
NC_000004.11:g.88903646C>G , CM000666.1:g.88903646C>G	GRCh37
NC_000004.10:g.89122670C>G	NCBI36
NG_030362.1:g.11845C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.420C>G	ENSP00000422973.2:p.Tyr140Ter
ENST00000614857.5:c.543C>G	ENSP00000477824.2:p.Tyr181Ter
ENST00000681973.1:n.770C>G
ENST00000682026.1:n.496C>G
ENST00000682448.1:n.2029C>G
ENST00000682554.1:n.1991C>G
ENST00000682599.1:n.3031C>G
ENST00000682627.1:n.463C>G
ENST00000682865.1:n.827C>G
ENST00000683087.1:n.557C>G
ENST00000683168.1:n.1297C>G
ENST00000683620.1:n.1725C>G
ENST00000684106.1:n.2793C>G
ENST00000684450.1:n.1602C>G
ENST00000684710.1:n.1834C>G
ENST00000395080.8:c.543C>G MANE Select	ENSP00000378517.3:p.Tyr181Ter
ENST00000237623.11:c.501C>G	ENSP00000237623.7:p.Tyr167Ter
ENST00000360804.4:c.462C>G	ENSP00000354042.4:p.Tyr154Ter
ENST00000395080.7:c.543C>G	ENSP00000378517.3:p.Tyr181Ter
ENST00000508233.5:c.420C>G	ENSP00000422973.1:p.Tyr140Ter
ENST00000509659.5:n.832C>G
ENST00000614857.4:c.477C>G	ENSP00000477824.1:p.Tyr159Ter
NM_000582.2:c.501C>G	NP_000573.1:p.Tyr167Ter
NM_001040058.1:c.543C>G	NP_001035147.1:p.Tyr181Ter
NM_001040060.1:c.462C>G	NP_001035149.1:p.Tyr154Ter
NM_001251829.1:c.420C>G	NP_001238758.1:p.Tyr140Ter
NM_001251830.1:c.582C>G	NP_001238759.1:p.Tyr194Ter
NM_001040058.2:c.543C>G MANE Select	NP_001035147.1:p.Tyr181Ter
NM_000582.3:c.501C>G	NP_000573.1:p.Tyr167Ter
NM_001040060.2:c.462C>G	NP_001035149.1:p.Tyr154Ter
NM_001251829.2:c.420C>G	NP_001238758.1:p.Tyr140Ter
NM_001251830.2:c.582C>G	NP_001238759.1:p.Tyr194Ter