Canonical Allele Identifier: CA1474550878
Gene: SPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87982073C= , CM000666.2:g.87982073C= GRCh38
NC_000004.11:g.88903225C= , CM000666.1:g.88903225C= GRCh37
NC_000004.10:g.89122249C= NCBI36
NG_030362.1:g.11424C=

Transcript Alleles

HGVS Amino-acid change
ENST00000508233.6:c.417+275C= ENSP00000422973.2:n.417+275C=
ENST00000614857.5:c.540+275C= ENSP00000477824.2:n.540+275C=
ENST00000681973.1:n.767+275C=
ENST00000682026.1:n.493+275C=
ENST00000682448.1:n.2026+275C=
ENST00000682554.1:n.1988+275C=
ENST00000682599.1:n.3028+275C=
ENST00000682627.1:n.460+275C=
ENST00000682865.1:n.824+275C=
ENST00000683087.1:n.554+275C=
ENST00000683168.1:n.1294+275C=
ENST00000683620.1:n.1722+275C=
ENST00000684106.1:n.2790+275C=
ENST00000684450.1:n.1599+275C=
ENST00000684710.1:n.1831+275C=
ENST00000395080.8:c.540+275C= MANE Select ENSP00000378517.3:n.540+275C=
ENST00000237623.11:c.498+275C= ENSP00000237623.7:n.498+275C=
ENST00000360804.4:c.459+275C= ENSP00000354042.4:n.459+275C=
ENST00000395080.7:c.540+275C= ENSP00000378517.3:n.540+275C=
ENST00000508233.5:c.417+275C= ENSP00000422973.1:n.417+275C=
ENST00000509659.5:n.829+275C=
ENST00000614857.4:c.474+275C= ENSP00000477824.1:n.474+275C=
NM_000582.2:c.498+275C= NP_000573.1:n.498+275C=
NM_001040058.1:c.540+275C= NP_001035147.1:n.540+275C=
NM_001040060.1:c.459+275C= NP_001035149.1:n.459+275C=
NM_001251829.1:c.417+275C= NP_001238758.1:n.417+275C=
NM_001251830.1:c.579+275C= NP_001238759.1:n.579+275C=
NM_001040058.2:c.540+275C= MANE Select NP_001035147.1:n.540+275C=
NM_000582.3:c.498+275C= NP_000573.1:n.498+275C=
NM_001040060.2:c.459+275C= NP_001035149.1:n.459+275C=
NM_001251829.2:c.417+275C= NP_001238758.1:n.417+275C=
NM_001251830.2:c.579+275C= NP_001238759.1:n.579+275C=