Canonical Allele Identifier: CA440296395

Gene: SPP1

Linked Data

• gnomAD v4: 4-87982512-G-A
• MyVariant Identifiers: chr4:g.88903664G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982512G>A , CM000666.2:g.87982512G>A	GRCh38
NC_000004.11:g.88903664G>A , CM000666.1:g.88903664G>A	GRCh37
NC_000004.10:g.89122688G>A	NCBI36
NG_030362.1:g.11863G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.438G>A	ENSP00000422973.2:p.Glu146=
ENST00000614857.5:c.561G>A	ENSP00000477824.2:p.Glu187=
ENST00000681973.1:n.788G>A
ENST00000682026.1:n.514G>A
ENST00000682448.1:n.2047G>A
ENST00000682554.1:n.2009G>A
ENST00000682599.1:n.3049G>A
ENST00000682627.1:n.481G>A
ENST00000682865.1:n.845G>A
ENST00000683087.1:n.575G>A
ENST00000683168.1:n.1315G>A
ENST00000683620.1:n.1743G>A
ENST00000684106.1:n.2811G>A
ENST00000684450.1:n.1620G>A
ENST00000684710.1:n.1852G>A
ENST00000395080.8:c.561G>A MANE Select	ENSP00000378517.3:p.Glu187=
ENST00000237623.11:c.519G>A	ENSP00000237623.7:p.Glu173=
ENST00000360804.4:c.480G>A	ENSP00000354042.4:p.Glu160=
ENST00000395080.7:c.561G>A	ENSP00000378517.3:p.Glu187=
ENST00000508233.5:c.438G>A	ENSP00000422973.1:p.Glu146=
ENST00000509659.5:n.850G>A
ENST00000614857.4:c.495G>A	ENSP00000477824.1:p.Glu165=
NM_000582.2:c.519G>A	NP_000573.1:p.Glu173=
NM_001040058.1:c.561G>A	NP_001035147.1:p.Glu187=
NM_001040060.1:c.480G>A	NP_001035149.1:p.Glu160=
NM_001251829.1:c.438G>A	NP_001238758.1:p.Glu146=
NM_001251830.1:c.600G>A	NP_001238759.1:p.Glu200=
NM_001040058.2:c.561G>A MANE Select	NP_001035147.1:p.Glu187=
NM_000582.3:c.519G>A	NP_000573.1:p.Glu173=
NM_001040060.2:c.480G>A	NP_001035149.1:p.Glu160=
NM_001251829.2:c.438G>A	NP_001238758.1:p.Glu146=
NM_001251830.2:c.600G>A	NP_001238759.1:p.Glu200=