Canonical Allele Identifier: CA357618199

Gene: SPP1

Linked Data

• dbSNP Id: rs1454329666
• MyVariant Identifiers: chr4:g.88903654C>T (hg19) ; chr4:g.87982502C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982502C>T , CM000666.2:g.87982502C>T	GRCh38
NC_000004.11:g.88903654C>T , CM000666.1:g.88903654C>T	GRCh37
NC_000004.10:g.89122678C>T	NCBI36
NG_030362.1:g.11853C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.428C>T	ENSP00000422973.2:p.Ala143Val
ENST00000614857.5:c.551C>T	ENSP00000477824.2:p.Ala184Val
ENST00000681973.1:n.778C>T
ENST00000682026.1:n.504C>T
ENST00000682448.1:n.2037C>T
ENST00000682554.1:n.1999C>T
ENST00000682599.1:n.3039C>T
ENST00000682627.1:n.471C>T
ENST00000682865.1:n.835C>T
ENST00000683087.1:n.565C>T
ENST00000683168.1:n.1305C>T
ENST00000683620.1:n.1733C>T
ENST00000684106.1:n.2801C>T
ENST00000684450.1:n.1610C>T
ENST00000684710.1:n.1842C>T
ENST00000395080.8:c.551C>T MANE Select	ENSP00000378517.3:p.Ala184Val
ENST00000237623.11:c.509C>T	ENSP00000237623.7:p.Ala170Val
ENST00000360804.4:c.470C>T	ENSP00000354042.4:p.Ala157Val
ENST00000395080.7:c.551C>T	ENSP00000378517.3:p.Ala184Val
ENST00000508233.5:c.428C>T	ENSP00000422973.1:p.Ala143Val
ENST00000509659.5:n.840C>T
ENST00000614857.4:c.485C>T	ENSP00000477824.1:p.Ala162Val
NM_000582.2:c.509C>T	NP_000573.1:p.Ala170Val
NM_001040058.1:c.551C>T	NP_001035147.1:p.Ala184Val
NM_001040060.1:c.470C>T	NP_001035149.1:p.Ala157Val
NM_001251829.1:c.428C>T	NP_001238758.1:p.Ala143Val
NM_001251830.1:c.590C>T	NP_001238759.1:p.Ala197Val
NM_001040058.2:c.551C>T MANE Select	NP_001035147.1:p.Ala184Val
NM_000582.3:c.509C>T	NP_000573.1:p.Ala170Val
NM_001040060.2:c.470C>T	NP_001035149.1:p.Ala157Val
NM_001251829.2:c.428C>T	NP_001238758.1:p.Ala143Val
NM_001251830.2:c.590C>T	NP_001238759.1:p.Ala197Val