Canonical Allele Identifier: CA440296403

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903676A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982524A>C , CM000666.2:g.87982524A>C	GRCh38
NC_000004.11:g.88903676A>C , CM000666.1:g.88903676A>C	GRCh37
NC_000004.10:g.89122700A>C	NCBI36
NG_030362.1:g.11875A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.450A>C	ENSP00000422973.2:p.Ser150=
ENST00000614857.5:c.573A>C	ENSP00000477824.2:p.Ser191=
ENST00000681973.1:n.800A>C
ENST00000682026.1:n.526A>C
ENST00000682448.1:n.2059A>C
ENST00000682554.1:n.2021A>C
ENST00000682599.1:n.3061A>C
ENST00000682627.1:n.493A>C
ENST00000682865.1:n.857A>C
ENST00000683087.1:n.587A>C
ENST00000683168.1:n.1327A>C
ENST00000683620.1:n.1755A>C
ENST00000684106.1:n.2823A>C
ENST00000684450.1:n.1632A>C
ENST00000684710.1:n.1864A>C
ENST00000395080.8:c.573A>C MANE Select	ENSP00000378517.3:p.Ser191=
ENST00000237623.11:c.531A>C	ENSP00000237623.7:p.Ser177=
ENST00000360804.4:c.492A>C	ENSP00000354042.4:p.Ser164=
ENST00000395080.7:c.573A>C	ENSP00000378517.3:p.Ser191=
ENST00000508233.5:c.450A>C	ENSP00000422973.1:p.Ser150=
ENST00000509659.5:n.862A>C
ENST00000614857.4:c.507A>C	ENSP00000477824.1:p.Ser169=
NM_000582.2:c.531A>C	NP_000573.1:p.Ser177=
NM_001040058.1:c.573A>C	NP_001035147.1:p.Ser191=
NM_001040060.1:c.492A>C	NP_001035149.1:p.Ser164=
NM_001251829.1:c.450A>C	NP_001238758.1:p.Ser150=
NM_001251830.1:c.612A>C	NP_001238759.1:p.Ser204=
NM_001040058.2:c.573A>C MANE Select	NP_001035147.1:p.Ser191=
NM_000582.3:c.531A>C	NP_000573.1:p.Ser177=
NM_001040060.2:c.492A>C	NP_001035149.1:p.Ser164=
NM_001251829.2:c.450A>C	NP_001238758.1:p.Ser150=
NM_001251830.2:c.612A>C	NP_001238759.1:p.Ser204=