Canonical Allele Identifier: CA1474550933

Gene: SPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982210T= , CM000666.2:g.87982210T=	GRCh38
NC_000004.11:g.88903362T= , CM000666.1:g.88903362T=	GRCh37
NC_000004.10:g.89122386T=	NCBI36
NG_030362.1:g.11561T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.418-282T=	ENSP00000422973.2:n.418-282T=
ENST00000614857.5:c.541-282T=	ENSP00000477824.2:n.541-282T=
ENST00000681973.1:n.768-282T=
ENST00000682026.1:n.494-282T=
ENST00000682448.1:n.2027-282T=
ENST00000682554.1:n.1989-282T=
ENST00000682599.1:n.3029-282T=
ENST00000682627.1:n.461-282T=
ENST00000682865.1:n.825-282T=
ENST00000683087.1:n.555-282T=
ENST00000683168.1:n.1295-282T=
ENST00000683620.1:n.1723-282T=
ENST00000684106.1:n.2791-282T=
ENST00000684450.1:n.1600-282T=
ENST00000684710.1:n.1832-282T=
ENST00000395080.8:c.541-282T= MANE Select	ENSP00000378517.3:n.541-282T=
ENST00000237623.11:c.499-282T=	ENSP00000237623.7:n.499-282T=
ENST00000360804.4:c.460-282T=	ENSP00000354042.4:n.460-282T=
ENST00000395080.7:c.541-282T=	ENSP00000378517.3:n.541-282T=
ENST00000508233.5:c.418-282T=	ENSP00000422973.1:n.418-282T=
ENST00000509659.5:n.830-282T=
ENST00000614857.4:c.475-282T=	ENSP00000477824.1:n.475-282T=
NM_000582.2:c.499-282T=	NP_000573.1:n.499-282T=
NM_001040058.1:c.541-282T=	NP_001035147.1:n.541-282T=
NM_001040060.1:c.460-282T=	NP_001035149.1:n.460-282T=
NM_001251829.1:c.418-282T=	NP_001238758.1:n.418-282T=
NM_001251830.1:c.580-282T=	NP_001238759.1:n.580-282T=
NM_001040058.2:c.541-282T= MANE Select	NP_001035147.1:n.541-282T=
NM_000582.3:c.499-282T=	NP_000573.1:n.499-282T=
NM_001040060.2:c.460-282T=	NP_001035149.1:n.460-282T=
NM_001251829.2:c.418-282T=	NP_001238758.1:n.418-282T=
NM_001251830.2:c.580-282T=	NP_001238759.1:n.580-282T=