Canonical Allele Identifier: CA357618229

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903662G>T (hg19) ; chr4:g.87982510G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982510G>T , CM000666.2:g.87982510G>T	GRCh38
NC_000004.11:g.88903662G>T , CM000666.1:g.88903662G>T	GRCh37
NC_000004.10:g.89122686G>T	NCBI36
NG_030362.1:g.11861G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.436G>T	ENSP00000422973.2:p.Glu146Ter
ENST00000614857.5:c.559G>T	ENSP00000477824.2:p.Glu187Ter
ENST00000681973.1:n.786G>T
ENST00000682026.1:n.512G>T
ENST00000682448.1:n.2045G>T
ENST00000682554.1:n.2007G>T
ENST00000682599.1:n.3047G>T
ENST00000682627.1:n.479G>T
ENST00000682865.1:n.843G>T
ENST00000683087.1:n.573G>T
ENST00000683168.1:n.1313G>T
ENST00000683620.1:n.1741G>T
ENST00000684106.1:n.2809G>T
ENST00000684450.1:n.1618G>T
ENST00000684710.1:n.1850G>T
ENST00000395080.8:c.559G>T MANE Select	ENSP00000378517.3:p.Glu187Ter
ENST00000237623.11:c.517G>T	ENSP00000237623.7:p.Glu173Ter
ENST00000360804.4:c.478G>T	ENSP00000354042.4:p.Glu160Ter
ENST00000395080.7:c.559G>T	ENSP00000378517.3:p.Glu187Ter
ENST00000508233.5:c.436G>T	ENSP00000422973.1:p.Glu146Ter
ENST00000509659.5:n.848G>T
ENST00000614857.4:c.493G>T	ENSP00000477824.1:p.Glu165Ter
NM_000582.2:c.517G>T	NP_000573.1:p.Glu173Ter
NM_001040058.1:c.559G>T	NP_001035147.1:p.Glu187Ter
NM_001040060.1:c.478G>T	NP_001035149.1:p.Glu160Ter
NM_001251829.1:c.436G>T	NP_001238758.1:p.Glu146Ter
NM_001251830.1:c.598G>T	NP_001238759.1:p.Glu200Ter
NM_001040058.2:c.559G>T MANE Select	NP_001035147.1:p.Glu187Ter
NM_000582.3:c.517G>T	NP_000573.1:p.Glu173Ter
NM_001040060.2:c.478G>T	NP_001035149.1:p.Glu160Ter
NM_001251829.2:c.436G>T	NP_001238758.1:p.Glu146Ter
NM_001251830.2:c.598G>T	NP_001238759.1:p.Glu200Ter