Canonical Allele Identifier: CA357618301

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903679C>G (hg19) ; chr4:g.87982527C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982527C>G , CM000666.2:g.87982527C>G	GRCh38
NC_000004.11:g.88903679C>G , CM000666.1:g.88903679C>G	GRCh37
NC_000004.10:g.89122703C>G	NCBI36
NG_030362.1:g.11878C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.453C>G	ENSP00000422973.2:p.His151Gln
ENST00000614857.5:c.576C>G	ENSP00000477824.2:p.His192Gln
ENST00000681973.1:n.803C>G
ENST00000682026.1:n.529C>G
ENST00000682448.1:n.2062C>G
ENST00000682554.1:n.2024C>G
ENST00000682599.1:n.3064C>G
ENST00000682627.1:n.496C>G
ENST00000682865.1:n.860C>G
ENST00000683087.1:n.590C>G
ENST00000683168.1:n.1330C>G
ENST00000683620.1:n.1758C>G
ENST00000684106.1:n.2826C>G
ENST00000684450.1:n.1635C>G
ENST00000684710.1:n.1867C>G
ENST00000395080.8:c.576C>G MANE Select	ENSP00000378517.3:p.His192Gln
ENST00000237623.11:c.534C>G	ENSP00000237623.7:p.His178Gln
ENST00000360804.4:c.495C>G	ENSP00000354042.4:p.His165Gln
ENST00000395080.7:c.576C>G	ENSP00000378517.3:p.His192Gln
ENST00000508233.5:c.453C>G	ENSP00000422973.1:p.His151Gln
ENST00000509659.5:n.865C>G
ENST00000614857.4:c.510C>G	ENSP00000477824.1:p.His170Gln
NM_000582.2:c.534C>G	NP_000573.1:p.His178Gln
NM_001040058.1:c.576C>G	NP_001035147.1:p.His192Gln
NM_001040060.1:c.495C>G	NP_001035149.1:p.His165Gln
NM_001251829.1:c.453C>G	NP_001238758.1:p.His151Gln
NM_001251830.1:c.615C>G	NP_001238759.1:p.His205Gln
NM_001040058.2:c.576C>G MANE Select	NP_001035147.1:p.His192Gln
NM_000582.3:c.534C>G	NP_000573.1:p.His178Gln
NM_001040060.2:c.495C>G	NP_001035149.1:p.His165Gln
NM_001251829.2:c.453C>G	NP_001238758.1:p.His151Gln
NM_001251830.2:c.615C>G	NP_001238759.1:p.His205Gln