Canonical Allele Identifier: CA1474551068

Gene: SPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982496C= , CM000666.2:g.87982496C=	GRCh38
NC_000004.11:g.88903648C= , CM000666.1:g.88903648C=	GRCh37
NC_000004.10:g.89122672C=	NCBI36
NG_030362.1:g.11847C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.422C=	ENSP00000422973.2:p.Pro141=
ENST00000614857.5:c.545C=	ENSP00000477824.2:p.Pro182=
ENST00000681973.1:n.772C=
ENST00000682026.1:n.498C=
ENST00000682448.1:n.2031C=
ENST00000682554.1:n.1993C=
ENST00000682599.1:n.3033C=
ENST00000682627.1:n.465C=
ENST00000682865.1:n.829C=
ENST00000683087.1:n.559C=
ENST00000683168.1:n.1299C=
ENST00000683620.1:n.1727C=
ENST00000684106.1:n.2795C=
ENST00000684450.1:n.1604C=
ENST00000684710.1:n.1836C=
ENST00000395080.8:c.545C= MANE Select	ENSP00000378517.3:p.Pro182=
ENST00000237623.11:c.503C=	ENSP00000237623.7:p.Pro168=
ENST00000360804.4:c.464C=	ENSP00000354042.4:p.Pro155=
ENST00000395080.7:c.545C=	ENSP00000378517.3:p.Pro182=
ENST00000508233.5:c.422C=	ENSP00000422973.1:p.Pro141=
ENST00000509659.5:n.834C=
ENST00000614857.4:c.479C=	ENSP00000477824.1:p.Pro160=
NM_000582.2:c.503C=	NP_000573.1:p.Pro168=
NM_001040058.1:c.545C=	NP_001035147.1:p.Pro182=
NM_001040060.1:c.464C=	NP_001035149.1:p.Pro155=
NM_001251829.1:c.422C=	NP_001238758.1:p.Pro141=
NM_001251830.1:c.584C=	NP_001238759.1:p.Pro195=
NM_001040058.2:c.545C= MANE Select	NP_001035147.1:p.Pro182=
NM_000582.3:c.503C=	NP_000573.1:p.Pro168=
NM_001040060.2:c.464C=	NP_001035149.1:p.Pro155=
NM_001251829.2:c.422C=	NP_001238758.1:p.Pro141=
NM_001251830.2:c.584C=	NP_001238759.1:p.Pro195=