Canonical Allele Identifier: CA440296393

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903658A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982506A>T , CM000666.2:g.87982506A>T	GRCh38
NC_000004.11:g.88903658A>T , CM000666.1:g.88903658A>T	GRCh37
NC_000004.10:g.89122682A>T	NCBI36
NG_030362.1:g.11857A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.432A>T	ENSP00000422973.2:p.Thr144=
ENST00000614857.5:c.555A>T	ENSP00000477824.2:p.Thr185=
ENST00000681973.1:n.782A>T
ENST00000682026.1:n.508A>T
ENST00000682448.1:n.2041A>T
ENST00000682554.1:n.2003A>T
ENST00000682599.1:n.3043A>T
ENST00000682627.1:n.475A>T
ENST00000682865.1:n.839A>T
ENST00000683087.1:n.569A>T
ENST00000683168.1:n.1309A>T
ENST00000683620.1:n.1737A>T
ENST00000684106.1:n.2805A>T
ENST00000684450.1:n.1614A>T
ENST00000684710.1:n.1846A>T
ENST00000395080.8:c.555A>T MANE Select	ENSP00000378517.3:p.Thr185=
ENST00000237623.11:c.513A>T	ENSP00000237623.7:p.Thr171=
ENST00000360804.4:c.474A>T	ENSP00000354042.4:p.Thr158=
ENST00000395080.7:c.555A>T	ENSP00000378517.3:p.Thr185=
ENST00000508233.5:c.432A>T	ENSP00000422973.1:p.Thr144=
ENST00000509659.5:n.844A>T
ENST00000614857.4:c.489A>T	ENSP00000477824.1:p.Thr163=
NM_000582.2:c.513A>T	NP_000573.1:p.Thr171=
NM_001040058.1:c.555A>T	NP_001035147.1:p.Thr185=
NM_001040060.1:c.474A>T	NP_001035149.1:p.Thr158=
NM_001251829.1:c.432A>T	NP_001238758.1:p.Thr144=
NM_001251830.1:c.594A>T	NP_001238759.1:p.Thr198=
NM_001040058.2:c.555A>T MANE Select	NP_001035147.1:p.Thr185=
NM_000582.3:c.513A>T	NP_000573.1:p.Thr171=
NM_001040060.2:c.474A>T	NP_001035149.1:p.Thr158=
NM_001251829.2:c.432A>T	NP_001238758.1:p.Thr144=
NM_001251830.2:c.594A>T	NP_001238759.1:p.Thr198=