Canonical Allele Identifier: CA1474550861

Gene: SPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982032C= , CM000666.2:g.87982032C=	GRCh38
NC_000004.11:g.88903184C= , CM000666.1:g.88903184C=	GRCh37
NC_000004.10:g.89122208C=	NCBI36
NG_030362.1:g.11383C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000508233.6:c.417+234C=	ENSP00000422973.2:n.417+234C=
ENST00000614857.5:c.540+234C=	ENSP00000477824.2:n.540+234C=
ENST00000681973.1:n.767+234C=
ENST00000682026.1:n.493+234C=
ENST00000682448.1:n.2026+234C=
ENST00000682554.1:n.1988+234C=
ENST00000682599.1:n.3028+234C=
ENST00000682627.1:n.460+234C=
ENST00000682865.1:n.824+234C=
ENST00000683087.1:n.554+234C=
ENST00000683168.1:n.1294+234C=
ENST00000683620.1:n.1722+234C=
ENST00000684106.1:n.2790+234C=
ENST00000684450.1:n.1599+234C=
ENST00000684710.1:n.1831+234C=
ENST00000395080.8:c.540+234C= MANE Select	ENSP00000378517.3:n.540+234C=
ENST00000237623.11:c.498+234C=	ENSP00000237623.7:n.498+234C=
ENST00000360804.4:c.459+234C=	ENSP00000354042.4:n.459+234C=
ENST00000395080.7:c.540+234C=	ENSP00000378517.3:n.540+234C=
ENST00000508233.5:c.417+234C=	ENSP00000422973.1:n.417+234C=
ENST00000509659.5:n.829+234C=
ENST00000614857.4:c.474+234C=	ENSP00000477824.1:n.474+234C=
NM_000582.2:c.498+234C=	NP_000573.1:n.498+234C=
NM_001040058.1:c.540+234C=	NP_001035147.1:n.540+234C=
NM_001040060.1:c.459+234C=	NP_001035149.1:n.459+234C=
NM_001251829.1:c.417+234C=	NP_001238758.1:n.417+234C=
NM_001251830.1:c.579+234C=	NP_001238759.1:n.579+234C=
NM_001040058.2:c.540+234C= MANE Select	NP_001035147.1:n.540+234C=
NM_000582.3:c.498+234C=	NP_000573.1:n.498+234C=
NM_001040060.2:c.459+234C=	NP_001035149.1:n.459+234C=
NM_001251829.2:c.417+234C=	NP_001238758.1:n.417+234C=
NM_001251830.2:c.579+234C=	NP_001238759.1:n.579+234C=