Canonical Allele Identifier: CA357618257

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903668A>G (hg19) ; chr4:g.87982516A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982516A>G , CM000666.2:g.87982516A>G	GRCh38
NC_000004.11:g.88903668A>G , CM000666.1:g.88903668A>G	GRCh37
NC_000004.10:g.89122692A>G	NCBI36
NG_030362.1:g.11867A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.442A>G	ENSP00000422973.2:p.Ile148Val
ENST00000614857.5:c.565A>G	ENSP00000477824.2:p.Ile189Val
ENST00000681973.1:n.792A>G
ENST00000682026.1:n.518A>G
ENST00000682448.1:n.2051A>G
ENST00000682554.1:n.2013A>G
ENST00000682599.1:n.3053A>G
ENST00000682627.1:n.485A>G
ENST00000682865.1:n.849A>G
ENST00000683087.1:n.579A>G
ENST00000683168.1:n.1319A>G
ENST00000683620.1:n.1747A>G
ENST00000684106.1:n.2815A>G
ENST00000684450.1:n.1624A>G
ENST00000684710.1:n.1856A>G
ENST00000395080.8:c.565A>G MANE Select	ENSP00000378517.3:p.Ile189Val
ENST00000237623.11:c.523A>G	ENSP00000237623.7:p.Ile175Val
ENST00000360804.4:c.484A>G	ENSP00000354042.4:p.Ile162Val
ENST00000395080.7:c.565A>G	ENSP00000378517.3:p.Ile189Val
ENST00000508233.5:c.442A>G	ENSP00000422973.1:p.Ile148Val
ENST00000509659.5:n.854A>G
ENST00000614857.4:c.499A>G	ENSP00000477824.1:p.Ile167Val
NM_000582.2:c.523A>G	NP_000573.1:p.Ile175Val
NM_001040058.1:c.565A>G	NP_001035147.1:p.Ile189Val
NM_001040060.1:c.484A>G	NP_001035149.1:p.Ile162Val
NM_001251829.1:c.442A>G	NP_001238758.1:p.Ile148Val
NM_001251830.1:c.604A>G	NP_001238759.1:p.Ile202Val
NM_001040058.2:c.565A>G MANE Select	NP_001035147.1:p.Ile189Val
NM_000582.3:c.523A>G	NP_000573.1:p.Ile175Val
NM_001040060.2:c.484A>G	NP_001035149.1:p.Ile162Val
NM_001251829.2:c.442A>G	NP_001238758.1:p.Ile148Val
NM_001251830.2:c.604A>G	NP_001238759.1:p.Ile202Val