Canonical Allele Identifier: CA357618259

Gene: SPP1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.442A>T	ENSP00000422973.2:p.Ile148Phe
ENST00000614857.5:c.565A>T	ENSP00000477824.2:p.Ile189Phe
ENST00000681973.1:n.792A>T
ENST00000682026.1:n.518A>T
ENST00000682448.1:n.2051A>T
ENST00000682554.1:n.2013A>T
ENST00000682599.1:n.3053A>T
ENST00000682627.1:n.485A>T
ENST00000682865.1:n.849A>T
ENST00000683087.1:n.579A>T
ENST00000683168.1:n.1319A>T
ENST00000683620.1:n.1747A>T
ENST00000684106.1:n.2815A>T
ENST00000684450.1:n.1624A>T
ENST00000684710.1:n.1856A>T
ENST00000395080.8:c.565A>T MANE Select	ENSP00000378517.3:p.Ile189Phe
ENST00000237623.11:c.523A>T	ENSP00000237623.7:p.Ile175Phe
ENST00000360804.4:c.484A>T	ENSP00000354042.4:p.Ile162Phe
ENST00000395080.7:c.565A>T	ENSP00000378517.3:p.Ile189Phe
ENST00000508233.5:c.442A>T	ENSP00000422973.1:p.Ile148Phe
ENST00000509659.5:n.854A>T
ENST00000614857.4:c.499A>T	ENSP00000477824.1:p.Ile167Phe
NM_000582.2:c.523A>T	NP_000573.1:p.Ile175Phe
NM_001040058.1:c.565A>T	NP_001035147.1:p.Ile189Phe
NM_001040060.1:c.484A>T	NP_001035149.1:p.Ile162Phe
NM_001251829.1:c.442A>T	NP_001238758.1:p.Ile148Phe
NM_001251830.1:c.604A>T	NP_001238759.1:p.Ile202Phe
NM_001040058.2:c.565A>T MANE Select	NP_001035147.1:p.Ile189Phe
NM_000582.3:c.523A>T	NP_000573.1:p.Ile175Phe
NM_001040060.2:c.484A>T	NP_001035149.1:p.Ile162Phe
NM_001251829.2:c.442A>T	NP_001238758.1:p.Ile148Phe
NM_001251830.2:c.604A>T	NP_001238759.1:p.Ile202Phe