Canonical Allele Identifier: CA3003618

Gene: SPP1

Linked Data

• dbSNP Id: rs534065695
• ExAC: 4:88903661 C / T
• gnomAD v2: 4-88903661-C-T
• gnomAD v3: 4-87982509-C-T
• gnomAD v4: 4-87982509-C-T
• COSMIC: COSM2957281
• MyVariant Identifiers: chr4:g.88903661C>T (hg19) ; chr4:g.87982509C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982509C>T , CM000666.2:g.87982509C>T	GRCh38
NC_000004.11:g.88903661C>T , CM000666.1:g.88903661C>T	GRCh37
NC_000004.10:g.89122685C>T	NCBI36
NG_030362.1:g.11860C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.435C>T	ENSP00000422973.2:p.Asp145=
ENST00000614857.5:c.558C>T	ENSP00000477824.2:p.Asp186=
ENST00000681973.1:n.785C>T
ENST00000682026.1:n.511C>T
ENST00000682448.1:n.2044C>T
ENST00000682554.1:n.2006C>T
ENST00000682599.1:n.3046C>T
ENST00000682627.1:n.478C>T
ENST00000682865.1:n.842C>T
ENST00000683087.1:n.572C>T
ENST00000683168.1:n.1312C>T
ENST00000683620.1:n.1740C>T
ENST00000684106.1:n.2808C>T
ENST00000684450.1:n.1617C>T
ENST00000684710.1:n.1849C>T
ENST00000395080.8:c.558C>T MANE Select	ENSP00000378517.3:p.Asp186=
ENST00000237623.11:c.516C>T	ENSP00000237623.7:p.Asp172=
ENST00000360804.4:c.477C>T	ENSP00000354042.4:p.Asp159=
ENST00000395080.7:c.558C>T	ENSP00000378517.3:p.Asp186=
ENST00000508233.5:c.435C>T	ENSP00000422973.1:p.Asp145=
ENST00000509659.5:n.847C>T
ENST00000614857.4:c.492C>T	ENSP00000477824.1:p.Asp164=
NM_000582.2:c.516C>T	NP_000573.1:p.Asp172=
NM_001040058.1:c.558C>T	NP_001035147.1:p.Asp186=
NM_001040060.1:c.477C>T	NP_001035149.1:p.Asp159=
NM_001251829.1:c.435C>T	NP_001238758.1:p.Asp145=
NM_001251830.1:c.597C>T	NP_001238759.1:p.Asp199=
NM_001040058.2:c.558C>T MANE Select	NP_001035147.1:p.Asp186=
NM_000582.3:c.516C>T	NP_000573.1:p.Asp172=
NM_001040060.2:c.477C>T	NP_001035149.1:p.Asp159=
NM_001251829.2:c.435C>T	NP_001238758.1:p.Asp145=
NM_001251830.2:c.597C>T	NP_001238759.1:p.Asp199=