Canonical Allele Identifier: CA357618298

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903678A>C (hg19) ; chr4:g.87982526A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982526A>C , CM000666.2:g.87982526A>C	GRCh38
NC_000004.11:g.88903678A>C , CM000666.1:g.88903678A>C	GRCh37
NC_000004.10:g.89122702A>C	NCBI36
NG_030362.1:g.11877A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.452A>C	ENSP00000422973.2:p.His151Pro
ENST00000614857.5:c.575A>C	ENSP00000477824.2:p.His192Pro
ENST00000681973.1:n.802A>C
ENST00000682026.1:n.528A>C
ENST00000682448.1:n.2061A>C
ENST00000682554.1:n.2023A>C
ENST00000682599.1:n.3063A>C
ENST00000682627.1:n.495A>C
ENST00000682865.1:n.859A>C
ENST00000683087.1:n.589A>C
ENST00000683168.1:n.1329A>C
ENST00000683620.1:n.1757A>C
ENST00000684106.1:n.2825A>C
ENST00000684450.1:n.1634A>C
ENST00000684710.1:n.1866A>C
ENST00000395080.8:c.575A>C MANE Select	ENSP00000378517.3:p.His192Pro
ENST00000237623.11:c.533A>C	ENSP00000237623.7:p.His178Pro
ENST00000360804.4:c.494A>C	ENSP00000354042.4:p.His165Pro
ENST00000395080.7:c.575A>C	ENSP00000378517.3:p.His192Pro
ENST00000508233.5:c.452A>C	ENSP00000422973.1:p.His151Pro
ENST00000509659.5:n.864A>C
ENST00000614857.4:c.509A>C	ENSP00000477824.1:p.His170Pro
NM_000582.2:c.533A>C	NP_000573.1:p.His178Pro
NM_001040058.1:c.575A>C	NP_001035147.1:p.His192Pro
NM_001040060.1:c.494A>C	NP_001035149.1:p.His165Pro
NM_001251829.1:c.452A>C	NP_001238758.1:p.His151Pro
NM_001251830.1:c.614A>C	NP_001238759.1:p.His205Pro
NM_001040058.2:c.575A>C MANE Select	NP_001035147.1:p.His192Pro
NM_000582.3:c.533A>C	NP_000573.1:p.His178Pro
NM_001040060.2:c.494A>C	NP_001035149.1:p.His165Pro
NM_001251829.2:c.452A>C	NP_001238758.1:p.His151Pro
NM_001251830.2:c.614A>C	NP_001238759.1:p.His205Pro