Canonical Allele Identifier: CA357618158

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903645A>C (hg19) ; chr4:g.87982493A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982493A>C , CM000666.2:g.87982493A>C	GRCh38
NC_000004.11:g.88903645A>C , CM000666.1:g.88903645A>C	GRCh37
NC_000004.10:g.89122669A>C	NCBI36
NG_030362.1:g.11844A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.419A>C	ENSP00000422973.2:p.Tyr140Ser
ENST00000614857.5:c.542A>C	ENSP00000477824.2:p.Tyr181Ser
ENST00000681973.1:n.769A>C
ENST00000682026.1:n.495A>C
ENST00000682448.1:n.2028A>C
ENST00000682554.1:n.1990A>C
ENST00000682599.1:n.3030A>C
ENST00000682627.1:n.462A>C
ENST00000682865.1:n.826A>C
ENST00000683087.1:n.556A>C
ENST00000683168.1:n.1296A>C
ENST00000683620.1:n.1724A>C
ENST00000684106.1:n.2792A>C
ENST00000684450.1:n.1601A>C
ENST00000684710.1:n.1833A>C
ENST00000395080.8:c.542A>C MANE Select	ENSP00000378517.3:p.Tyr181Ser
ENST00000237623.11:c.500A>C	ENSP00000237623.7:p.Tyr167Ser
ENST00000360804.4:c.461A>C	ENSP00000354042.4:p.Tyr154Ser
ENST00000395080.7:c.542A>C	ENSP00000378517.3:p.Tyr181Ser
ENST00000508233.5:c.419A>C	ENSP00000422973.1:p.Tyr140Ser
ENST00000509659.5:n.831A>C
ENST00000614857.4:c.476A>C	ENSP00000477824.1:p.Tyr159Ser
NM_000582.2:c.500A>C	NP_000573.1:p.Tyr167Ser
NM_001040058.1:c.542A>C	NP_001035147.1:p.Tyr181Ser
NM_001040060.1:c.461A>C	NP_001035149.1:p.Tyr154Ser
NM_001251829.1:c.419A>C	NP_001238758.1:p.Tyr140Ser
NM_001251830.1:c.581A>C	NP_001238759.1:p.Tyr194Ser
NM_001040058.2:c.542A>C MANE Select	NP_001035147.1:p.Tyr181Ser
NM_000582.3:c.500A>C	NP_000573.1:p.Tyr167Ser
NM_001040060.2:c.461A>C	NP_001035149.1:p.Tyr154Ser
NM_001251829.2:c.419A>C	NP_001238758.1:p.Tyr140Ser
NM_001251830.2:c.581A>C	NP_001238759.1:p.Tyr194Ser