Canonical Allele Identifier: CA1474551081

Gene: SPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982528A= , CM000666.2:g.87982528A=	GRCh38
NC_000004.11:g.88903680A= , CM000666.1:g.88903680A=	GRCh37
NC_000004.10:g.89122704A=	NCBI36
NG_030362.1:g.11879A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.454A=	ENSP00000422973.2:p.Met152=
ENST00000614857.5:c.577A=	ENSP00000477824.2:p.Met193=
ENST00000681973.1:n.804A=
ENST00000682026.1:n.530A=
ENST00000682448.1:n.2063A=
ENST00000682554.1:n.2025A=
ENST00000682599.1:n.3065A=
ENST00000682627.1:n.497A=
ENST00000682865.1:n.861A=
ENST00000683087.1:n.591A=
ENST00000683168.1:n.1331A=
ENST00000683620.1:n.1759A=
ENST00000684106.1:n.2827A=
ENST00000684450.1:n.1636A=
ENST00000684710.1:n.1868A=
ENST00000395080.8:c.577A= MANE Select	ENSP00000378517.3:p.Met193=
ENST00000237623.11:c.535A=	ENSP00000237623.7:p.Met179=
ENST00000360804.4:c.496A=	ENSP00000354042.4:p.Met166=
ENST00000395080.7:c.577A=	ENSP00000378517.3:p.Met193=
ENST00000508233.5:c.454A=	ENSP00000422973.1:p.Met152=
ENST00000509659.5:n.866A=
ENST00000614857.4:c.511A=	ENSP00000477824.1:p.Met171=
NM_000582.2:c.535A=	NP_000573.1:p.Met179=
NM_001040058.1:c.577A=	NP_001035147.1:p.Met193=
NM_001040060.1:c.496A=	NP_001035149.1:p.Met166=
NM_001251829.1:c.454A=	NP_001238758.1:p.Met152=
NM_001251830.1:c.616A=	NP_001238759.1:p.Met206=
NM_001040058.2:c.577A= MANE Select	NP_001035147.1:p.Met193=
NM_000582.3:c.535A=	NP_000573.1:p.Met179=
NM_001040060.2:c.496A=	NP_001035149.1:p.Met166=
NM_001251829.2:c.454A=	NP_001238758.1:p.Met152=
NM_001251830.2:c.616A=	NP_001238759.1:p.Met206=