Canonical Allele Identifier: CA1474551080

Gene: SPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982527C= , CM000666.2:g.87982527C=	GRCh38
NC_000004.11:g.88903679C= , CM000666.1:g.88903679C=	GRCh37
NC_000004.10:g.89122703C=	NCBI36
NG_030362.1:g.11878C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.453C=	ENSP00000422973.2:p.His151=
ENST00000614857.5:c.576C=	ENSP00000477824.2:p.His192=
ENST00000681973.1:n.803C=
ENST00000682026.1:n.529C=
ENST00000682448.1:n.2062C=
ENST00000682554.1:n.2024C=
ENST00000682599.1:n.3064C=
ENST00000682627.1:n.496C=
ENST00000682865.1:n.860C=
ENST00000683087.1:n.590C=
ENST00000683168.1:n.1330C=
ENST00000683620.1:n.1758C=
ENST00000684106.1:n.2826C=
ENST00000684450.1:n.1635C=
ENST00000684710.1:n.1867C=
ENST00000395080.8:c.576C= MANE Select	ENSP00000378517.3:p.His192=
ENST00000237623.11:c.534C=	ENSP00000237623.7:p.His178=
ENST00000360804.4:c.495C=	ENSP00000354042.4:p.His165=
ENST00000395080.7:c.576C=	ENSP00000378517.3:p.His192=
ENST00000508233.5:c.453C=	ENSP00000422973.1:p.His151=
ENST00000509659.5:n.865C=
ENST00000614857.4:c.510C=	ENSP00000477824.1:p.His170=
NM_000582.2:c.534C=	NP_000573.1:p.His178=
NM_001040058.1:c.576C=	NP_001035147.1:p.His192=
NM_001040060.1:c.495C=	NP_001035149.1:p.His165=
NM_001251829.1:c.453C=	NP_001238758.1:p.His151=
NM_001251830.1:c.615C=	NP_001238759.1:p.His205=
NM_001040058.2:c.576C= MANE Select	NP_001035147.1:p.His192=
NM_000582.3:c.534C=	NP_000573.1:p.His178=
NM_001040060.2:c.495C=	NP_001035149.1:p.His165=
NM_001251829.2:c.453C=	NP_001238758.1:p.His151=
NM_001251830.2:c.615C=	NP_001238759.1:p.His205=