Canonical Allele Identifier: CA100858263

Gene: SPP1

Linked Data

• dbSNP Id: rs1056417647
• MyVariant Identifiers: chr4:g.88903667C>T (hg19) ; chr4:g.87982515C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982515C>T , CM000666.2:g.87982515C>T	GRCh38
NC_000004.11:g.88903667C>T , CM000666.1:g.88903667C>T	GRCh37
NC_000004.10:g.89122691C>T	NCBI36
NG_030362.1:g.11866C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.441C>T	ENSP00000422973.2:p.Asp147=
ENST00000614857.5:c.564C>T	ENSP00000477824.2:p.Asp188=
ENST00000681973.1:n.791C>T
ENST00000682026.1:n.517C>T
ENST00000682448.1:n.2050C>T
ENST00000682554.1:n.2012C>T
ENST00000682599.1:n.3052C>T
ENST00000682627.1:n.484C>T
ENST00000682865.1:n.848C>T
ENST00000683087.1:n.578C>T
ENST00000683168.1:n.1318C>T
ENST00000683620.1:n.1746C>T
ENST00000684106.1:n.2814C>T
ENST00000684450.1:n.1623C>T
ENST00000684710.1:n.1855C>T
ENST00000395080.8:c.564C>T MANE Select	ENSP00000378517.3:p.Asp188=
ENST00000237623.11:c.522C>T	ENSP00000237623.7:p.Asp174=
ENST00000360804.4:c.483C>T	ENSP00000354042.4:p.Asp161=
ENST00000395080.7:c.564C>T	ENSP00000378517.3:p.Asp188=
ENST00000508233.5:c.441C>T	ENSP00000422973.1:p.Asp147=
ENST00000509659.5:n.853C>T
ENST00000614857.4:c.498C>T	ENSP00000477824.1:p.Asp166=
NM_000582.2:c.522C>T	NP_000573.1:p.Asp174=
NM_001040058.1:c.564C>T	NP_001035147.1:p.Asp188=
NM_001040060.1:c.483C>T	NP_001035149.1:p.Asp161=
NM_001251829.1:c.441C>T	NP_001238758.1:p.Asp147=
NM_001251830.1:c.603C>T	NP_001238759.1:p.Asp201=
NM_001040058.2:c.564C>T MANE Select	NP_001035147.1:p.Asp188=
NM_000582.3:c.522C>T	NP_000573.1:p.Asp174=
NM_001040060.2:c.483C>T	NP_001035149.1:p.Asp161=
NM_001251829.2:c.441C>T	NP_001238758.1:p.Asp147=
NM_001251830.2:c.603C>T	NP_001238759.1:p.Asp201=