Canonical Allele Identifier: CA357618214

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903659G>T (hg19) ; chr4:g.87982507G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982507G>T , CM000666.2:g.87982507G>T	GRCh38
NC_000004.11:g.88903659G>T , CM000666.1:g.88903659G>T	GRCh37
NC_000004.10:g.89122683G>T	NCBI36
NG_030362.1:g.11858G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.433G>T	ENSP00000422973.2:p.Asp145Tyr
ENST00000614857.5:c.556G>T	ENSP00000477824.2:p.Asp186Tyr
ENST00000681973.1:n.783G>T
ENST00000682026.1:n.509G>T
ENST00000682448.1:n.2042G>T
ENST00000682554.1:n.2004G>T
ENST00000682599.1:n.3044G>T
ENST00000682627.1:n.476G>T
ENST00000682865.1:n.840G>T
ENST00000683087.1:n.570G>T
ENST00000683168.1:n.1310G>T
ENST00000683620.1:n.1738G>T
ENST00000684106.1:n.2806G>T
ENST00000684450.1:n.1615G>T
ENST00000684710.1:n.1847G>T
ENST00000395080.8:c.556G>T MANE Select	ENSP00000378517.3:p.Asp186Tyr
ENST00000237623.11:c.514G>T	ENSP00000237623.7:p.Asp172Tyr
ENST00000360804.4:c.475G>T	ENSP00000354042.4:p.Asp159Tyr
ENST00000395080.7:c.556G>T	ENSP00000378517.3:p.Asp186Tyr
ENST00000508233.5:c.433G>T	ENSP00000422973.1:p.Asp145Tyr
ENST00000509659.5:n.845G>T
ENST00000614857.4:c.490G>T	ENSP00000477824.1:p.Asp164Tyr
NM_000582.2:c.514G>T	NP_000573.1:p.Asp172Tyr
NM_001040058.1:c.556G>T	NP_001035147.1:p.Asp186Tyr
NM_001040060.1:c.475G>T	NP_001035149.1:p.Asp159Tyr
NM_001251829.1:c.433G>T	NP_001238758.1:p.Asp145Tyr
NM_001251830.1:c.595G>T	NP_001238759.1:p.Asp199Tyr
NM_001040058.2:c.556G>T MANE Select	NP_001035147.1:p.Asp186Tyr
NM_000582.3:c.514G>T	NP_000573.1:p.Asp172Tyr
NM_001040060.2:c.475G>T	NP_001035149.1:p.Asp159Tyr
NM_001251829.2:c.433G>T	NP_001238758.1:p.Asp145Tyr
NM_001251830.2:c.595G>T	NP_001238759.1:p.Asp199Tyr