Canonical Allele Identifier: CA100857963
Gene: SPP1 HGNC NCBI

Linked Data

dbSNP Id: rs543360402
gnomAD v3: 4-87981964-C-A
gnomAD v4: 4-87981964-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87981964C>A , CM000666.2:g.87981964C>A GRCh38
NC_000004.11:g.88903116C>A , CM000666.1:g.88903116C>A GRCh37
NC_000004.10:g.89122140C>A NCBI36
NG_030362.1:g.11315C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000508233.6:c.417+166C>A ENSP00000422973.2:n.417+166C>A
ENST00000614857.5:c.540+166C>A ENSP00000477824.2:n.540+166C>A
ENST00000681973.1:n.767+166C>A
ENST00000682026.1:n.493+166C>A
ENST00000682448.1:n.2026+166C>A
ENST00000682554.1:n.1988+166C>A
ENST00000682599.1:n.3028+166C>A
ENST00000682627.1:n.460+166C>A
ENST00000682655.1:c.*127C>A ENSP00000508280.1:n.*127C>A
ENST00000682865.1:n.824+166C>A
ENST00000683087.1:n.554+166C>A
ENST00000683168.1:n.1294+166C>A
ENST00000683620.1:n.1722+166C>A
ENST00000684106.1:n.2790+166C>A
ENST00000684450.1:n.1599+166C>A
ENST00000684710.1:n.1831+166C>A
ENST00000395080.8:c.540+166C>A MANE Select ENSP00000378517.3:n.540+166C>A
ENST00000237623.11:c.498+166C>A ENSP00000237623.7:n.498+166C>A
ENST00000360804.4:c.459+166C>A ENSP00000354042.4:n.459+166C>A
ENST00000395080.7:c.540+166C>A ENSP00000378517.3:n.540+166C>A
ENST00000508233.5:c.417+166C>A ENSP00000422973.1:n.417+166C>A
ENST00000509659.5:n.829+166C>A
ENST00000614857.4:c.474+166C>A ENSP00000477824.1:n.474+166C>A
NM_000582.2:c.498+166C>A NP_000573.1:n.498+166C>A
NM_001040058.1:c.540+166C>A NP_001035147.1:n.540+166C>A
NM_001040060.1:c.459+166C>A NP_001035149.1:n.459+166C>A
NM_001251829.1:c.417+166C>A NP_001238758.1:n.417+166C>A
NM_001251830.1:c.579+166C>A NP_001238759.1:n.579+166C>A
NM_001040058.2:c.540+166C>A MANE Select NP_001035147.1:n.540+166C>A
NM_000582.3:c.498+166C>A NP_000573.1:n.498+166C>A
NM_001040060.2:c.459+166C>A NP_001035149.1:n.459+166C>A
NM_001251829.2:c.417+166C>A NP_001238758.1:n.417+166C>A
NM_001251830.2:c.579+166C>A NP_001238759.1:n.579+166C>A