Canonical Allele Identifier: CA100858079
Gene: SPP1 HGNC NCBI

Linked Data

dbSNP Id: rs776336930
gnomAD v2: 4-88903347-A-G
gnomAD v3: 4-87982195-A-G
gnomAD v4: 4-87982195-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87982195A>G , CM000666.2:g.87982195A>G GRCh38
NC_000004.11:g.88903347A>G , CM000666.1:g.88903347A>G GRCh37
NC_000004.10:g.89122371A>G NCBI36
NG_030362.1:g.11546A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000508233.6:c.418-297A>G ENSP00000422973.2:n.418-297A>G
ENST00000614857.5:c.541-297A>G ENSP00000477824.2:n.541-297A>G
ENST00000681973.1:n.768-297A>G
ENST00000682026.1:n.494-297A>G
ENST00000682448.1:n.2027-297A>G
ENST00000682554.1:n.1989-297A>G
ENST00000682599.1:n.3029-297A>G
ENST00000682627.1:n.461-297A>G
ENST00000682865.1:n.825-297A>G
ENST00000683087.1:n.555-297A>G
ENST00000683168.1:n.1295-297A>G
ENST00000683620.1:n.1723-297A>G
ENST00000684106.1:n.2791-297A>G
ENST00000684450.1:n.1600-297A>G
ENST00000684710.1:n.1832-297A>G
ENST00000395080.8:c.541-297A>G MANE Select ENSP00000378517.3:n.541-297A>G
ENST00000237623.11:c.499-297A>G ENSP00000237623.7:n.499-297A>G
ENST00000360804.4:c.460-297A>G ENSP00000354042.4:n.460-297A>G
ENST00000395080.7:c.541-297A>G ENSP00000378517.3:n.541-297A>G
ENST00000508233.5:c.418-297A>G ENSP00000422973.1:n.418-297A>G
ENST00000509659.5:n.830-297A>G
ENST00000614857.4:c.475-297A>G ENSP00000477824.1:n.475-297A>G
NM_000582.2:c.499-297A>G NP_000573.1:n.499-297A>G
NM_001040058.1:c.541-297A>G NP_001035147.1:n.541-297A>G
NM_001040060.1:c.460-297A>G NP_001035149.1:n.460-297A>G
NM_001251829.1:c.418-297A>G NP_001238758.1:n.418-297A>G
NM_001251830.1:c.580-297A>G NP_001238759.1:n.580-297A>G
NM_001040058.2:c.541-297A>G MANE Select NP_001035147.1:n.541-297A>G
NM_000582.3:c.499-297A>G NP_000573.1:n.499-297A>G
NM_001040060.2:c.460-297A>G NP_001035149.1:n.460-297A>G
NM_001251829.2:c.418-297A>G NP_001238758.1:n.418-297A>G
NM_001251830.2:c.580-297A>G NP_001238759.1:n.580-297A>G