Canonical Allele Identifier: CA357618172

Gene: SPP1

Linked Data

• dbSNP Id: rs1725687568
• COSMIC: COSM5931551
• MyVariant Identifiers: chr4:g.88903647C>T (hg19) ; chr4:g.87982495C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982495C>T , CM000666.2:g.87982495C>T	GRCh38
NC_000004.11:g.88903647C>T , CM000666.1:g.88903647C>T	GRCh37
NC_000004.10:g.89122671C>T	NCBI36
NG_030362.1:g.11846C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.421C>T	ENSP00000422973.2:p.Pro141Ser
ENST00000614857.5:c.544C>T	ENSP00000477824.2:p.Pro182Ser
ENST00000681973.1:n.771C>T
ENST00000682026.1:n.497C>T
ENST00000682448.1:n.2030C>T
ENST00000682554.1:n.1992C>T
ENST00000682599.1:n.3032C>T
ENST00000682627.1:n.464C>T
ENST00000682865.1:n.828C>T
ENST00000683087.1:n.558C>T
ENST00000683168.1:n.1298C>T
ENST00000683620.1:n.1726C>T
ENST00000684106.1:n.2794C>T
ENST00000684450.1:n.1603C>T
ENST00000684710.1:n.1835C>T
ENST00000395080.8:c.544C>T MANE Select	ENSP00000378517.3:p.Pro182Ser
ENST00000237623.11:c.502C>T	ENSP00000237623.7:p.Pro168Ser
ENST00000360804.4:c.463C>T	ENSP00000354042.4:p.Pro155Ser
ENST00000395080.7:c.544C>T	ENSP00000378517.3:p.Pro182Ser
ENST00000508233.5:c.421C>T	ENSP00000422973.1:p.Pro141Ser
ENST00000509659.5:n.833C>T
ENST00000614857.4:c.478C>T	ENSP00000477824.1:p.Pro160Ser
NM_000582.2:c.502C>T	NP_000573.1:p.Pro168Ser
NM_001040058.1:c.544C>T	NP_001035147.1:p.Pro182Ser
NM_001040060.1:c.463C>T	NP_001035149.1:p.Pro155Ser
NM_001251829.1:c.421C>T	NP_001238758.1:p.Pro141Ser
NM_001251830.1:c.583C>T	NP_001238759.1:p.Pro195Ser
NM_001040058.2:c.544C>T MANE Select	NP_001035147.1:p.Pro182Ser
NM_000582.3:c.502C>T	NP_000573.1:p.Pro168Ser
NM_001040060.2:c.463C>T	NP_001035149.1:p.Pro155Ser
NM_001251829.2:c.421C>T	NP_001238758.1:p.Pro141Ser
NM_001251830.2:c.583C>T	NP_001238759.1:p.Pro195Ser