Canonical Allele Identifier: CA1474550868
Gene: SPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87982052A= , CM000666.2:g.87982052A= GRCh38
NC_000004.11:g.88903204A= , CM000666.1:g.88903204A= GRCh37
NC_000004.10:g.89122228A= NCBI36
NG_030362.1:g.11403A=

Transcript Alleles

HGVS Amino-acid change
ENST00000508233.6:c.417+254A= ENSP00000422973.2:n.417+254A=
ENST00000614857.5:c.540+254A= ENSP00000477824.2:n.540+254A=
ENST00000681973.1:n.767+254A=
ENST00000682026.1:n.493+254A=
ENST00000682448.1:n.2026+254A=
ENST00000682554.1:n.1988+254A=
ENST00000682599.1:n.3028+254A=
ENST00000682627.1:n.460+254A=
ENST00000682865.1:n.824+254A=
ENST00000683087.1:n.554+254A=
ENST00000683168.1:n.1294+254A=
ENST00000683620.1:n.1722+254A=
ENST00000684106.1:n.2790+254A=
ENST00000684450.1:n.1599+254A=
ENST00000684710.1:n.1831+254A=
ENST00000395080.8:c.540+254A= MANE Select ENSP00000378517.3:n.540+254A=
ENST00000237623.11:c.498+254A= ENSP00000237623.7:n.498+254A=
ENST00000360804.4:c.459+254A= ENSP00000354042.4:n.459+254A=
ENST00000395080.7:c.540+254A= ENSP00000378517.3:n.540+254A=
ENST00000508233.5:c.417+254A= ENSP00000422973.1:n.417+254A=
ENST00000509659.5:n.829+254A=
ENST00000614857.4:c.474+254A= ENSP00000477824.1:n.474+254A=
NM_000582.2:c.498+254A= NP_000573.1:n.498+254A=
NM_001040058.1:c.540+254A= NP_001035147.1:n.540+254A=
NM_001040060.1:c.459+254A= NP_001035149.1:n.459+254A=
NM_001251829.1:c.417+254A= NP_001238758.1:n.417+254A=
NM_001251830.1:c.579+254A= NP_001238759.1:n.579+254A=
NM_001040058.2:c.540+254A= MANE Select NP_001035147.1:n.540+254A=
NM_000582.3:c.498+254A= NP_000573.1:n.498+254A=
NM_001040060.2:c.459+254A= NP_001035149.1:n.459+254A=
NM_001251829.2:c.417+254A= NP_001238758.1:n.417+254A=
NM_001251830.2:c.579+254A= NP_001238759.1:n.579+254A=