Canonical Allele Identifier: CA440296387

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903652T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982500T>C , CM000666.2:g.87982500T>C	GRCh38
NC_000004.11:g.88903652T>C , CM000666.1:g.88903652T>C	GRCh37
NC_000004.10:g.89122676T>C	NCBI36
NG_030362.1:g.11851T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.426T>C	ENSP00000422973.2:p.Asp142=
ENST00000614857.5:c.549T>C	ENSP00000477824.2:p.Asp183=
ENST00000681973.1:n.776T>C
ENST00000682026.1:n.502T>C
ENST00000682448.1:n.2035T>C
ENST00000682554.1:n.1997T>C
ENST00000682599.1:n.3037T>C
ENST00000682627.1:n.469T>C
ENST00000682865.1:n.833T>C
ENST00000683087.1:n.563T>C
ENST00000683168.1:n.1303T>C
ENST00000683620.1:n.1731T>C
ENST00000684106.1:n.2799T>C
ENST00000684450.1:n.1608T>C
ENST00000684710.1:n.1840T>C
ENST00000395080.8:c.549T>C MANE Select	ENSP00000378517.3:p.Asp183=
ENST00000237623.11:c.507T>C	ENSP00000237623.7:p.Asp169=
ENST00000360804.4:c.468T>C	ENSP00000354042.4:p.Asp156=
ENST00000395080.7:c.549T>C	ENSP00000378517.3:p.Asp183=
ENST00000508233.5:c.426T>C	ENSP00000422973.1:p.Asp142=
ENST00000509659.5:n.838T>C
ENST00000614857.4:c.483T>C	ENSP00000477824.1:p.Asp161=
NM_000582.2:c.507T>C	NP_000573.1:p.Asp169=
NM_001040058.1:c.549T>C	NP_001035147.1:p.Asp183=
NM_001040060.1:c.468T>C	NP_001035149.1:p.Asp156=
NM_001251829.1:c.426T>C	NP_001238758.1:p.Asp142=
NM_001251830.1:c.588T>C	NP_001238759.1:p.Asp196=
NM_001040058.2:c.549T>C MANE Select	NP_001035147.1:p.Asp183=
NM_000582.3:c.507T>C	NP_000573.1:p.Asp169=
NM_001040060.2:c.468T>C	NP_001035149.1:p.Asp156=
NM_001251829.2:c.426T>C	NP_001238758.1:p.Asp142=
NM_001251830.2:c.588T>C	NP_001238759.1:p.Asp196=