Canonical Allele Identifier: CA357618262

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903669T>G (hg19) ; chr4:g.87982517T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982517T>G , CM000666.2:g.87982517T>G	GRCh38
NC_000004.11:g.88903669T>G , CM000666.1:g.88903669T>G	GRCh37
NC_000004.10:g.89122693T>G	NCBI36
NG_030362.1:g.11868T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.443T>G	ENSP00000422973.2:p.Ile148Ser
ENST00000614857.5:c.566T>G	ENSP00000477824.2:p.Ile189Ser
ENST00000681973.1:n.793T>G
ENST00000682026.1:n.519T>G
ENST00000682448.1:n.2052T>G
ENST00000682554.1:n.2014T>G
ENST00000682599.1:n.3054T>G
ENST00000682627.1:n.486T>G
ENST00000682865.1:n.850T>G
ENST00000683087.1:n.580T>G
ENST00000683168.1:n.1320T>G
ENST00000683620.1:n.1748T>G
ENST00000684106.1:n.2816T>G
ENST00000684450.1:n.1625T>G
ENST00000684710.1:n.1857T>G
ENST00000395080.8:c.566T>G MANE Select	ENSP00000378517.3:p.Ile189Ser
ENST00000237623.11:c.524T>G	ENSP00000237623.7:p.Ile175Ser
ENST00000360804.4:c.485T>G	ENSP00000354042.4:p.Ile162Ser
ENST00000395080.7:c.566T>G	ENSP00000378517.3:p.Ile189Ser
ENST00000508233.5:c.443T>G	ENSP00000422973.1:p.Ile148Ser
ENST00000509659.5:n.855T>G
ENST00000614857.4:c.500T>G	ENSP00000477824.1:p.Ile167Ser
NM_000582.2:c.524T>G	NP_000573.1:p.Ile175Ser
NM_001040058.1:c.566T>G	NP_001035147.1:p.Ile189Ser
NM_001040060.1:c.485T>G	NP_001035149.1:p.Ile162Ser
NM_001251829.1:c.443T>G	NP_001238758.1:p.Ile148Ser
NM_001251830.1:c.605T>G	NP_001238759.1:p.Ile202Ser
NM_001040058.2:c.566T>G MANE Select	NP_001035147.1:p.Ile189Ser
NM_000582.3:c.524T>G	NP_000573.1:p.Ile175Ser
NM_001040060.2:c.485T>G	NP_001035149.1:p.Ile162Ser
NM_001251829.2:c.443T>G	NP_001238758.1:p.Ile148Ser
NM_001251830.2:c.605T>G	NP_001238759.1:p.Ile202Ser