Canonical Allele Identifier: CA357618168

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903647C>A (hg19) ; chr4:g.87982495C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.421C>A	ENSP00000422973.2:p.Pro141Thr
ENST00000614857.5:c.544C>A	ENSP00000477824.2:p.Pro182Thr
ENST00000681973.1:n.771C>A
ENST00000682026.1:n.497C>A
ENST00000682448.1:n.2030C>A
ENST00000682554.1:n.1992C>A
ENST00000682599.1:n.3032C>A
ENST00000682627.1:n.464C>A
ENST00000682865.1:n.828C>A
ENST00000683087.1:n.558C>A
ENST00000683168.1:n.1298C>A
ENST00000683620.1:n.1726C>A
ENST00000684106.1:n.2794C>A
ENST00000684450.1:n.1603C>A
ENST00000684710.1:n.1835C>A
ENST00000395080.8:c.544C>A MANE Select	ENSP00000378517.3:p.Pro182Thr
ENST00000237623.11:c.502C>A	ENSP00000237623.7:p.Pro168Thr
ENST00000360804.4:c.463C>A	ENSP00000354042.4:p.Pro155Thr
ENST00000395080.7:c.544C>A	ENSP00000378517.3:p.Pro182Thr
ENST00000508233.5:c.421C>A	ENSP00000422973.1:p.Pro141Thr
ENST00000509659.5:n.833C>A
ENST00000614857.4:c.478C>A	ENSP00000477824.1:p.Pro160Thr
NM_000582.2:c.502C>A	NP_000573.1:p.Pro168Thr
NM_001040058.1:c.544C>A	NP_001035147.1:p.Pro182Thr
NM_001040060.1:c.463C>A	NP_001035149.1:p.Pro155Thr
NM_001251829.1:c.421C>A	NP_001238758.1:p.Pro141Thr
NM_001251830.1:c.583C>A	NP_001238759.1:p.Pro195Thr
NM_001040058.2:c.544C>A MANE Select	NP_001035147.1:p.Pro182Thr
NM_000582.3:c.502C>A	NP_000573.1:p.Pro168Thr
NM_001040060.2:c.463C>A	NP_001035149.1:p.Pro155Thr
NM_001251829.2:c.421C>A	NP_001238758.1:p.Pro141Thr
NM_001251830.2:c.583C>A	NP_001238759.1:p.Pro195Thr