Canonical Allele Identifier: CA2671367355

Gene: SPP1

Linked Data

• gnomAD v4: 4-87982463-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982463A>G , CM000666.2:g.87982463A>G	GRCh38
NC_000004.11:g.88903615A>G , CM000666.1:g.88903615A>G	GRCh37
NC_000004.10:g.89122639A>G	NCBI36
NG_030362.1:g.11814A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.418-29A>G	ENSP00000422973.2:n.418-29A>G
ENST00000614857.5:c.541-29A>G	ENSP00000477824.2:n.541-29A>G
ENST00000681973.1:n.768-29A>G
ENST00000682026.1:n.494-29A>G
ENST00000682448.1:n.2027-29A>G
ENST00000682554.1:n.1989-29A>G
ENST00000682599.1:n.3029-29A>G
ENST00000682627.1:n.461-29A>G
ENST00000682865.1:n.825-29A>G
ENST00000683087.1:n.555-29A>G
ENST00000683168.1:n.1295-29A>G
ENST00000683620.1:n.1723-29A>G
ENST00000684106.1:n.2791-29A>G
ENST00000684450.1:n.1600-29A>G
ENST00000684710.1:n.1832-29A>G
ENST00000395080.8:c.541-29A>G MANE Select	ENSP00000378517.3:n.541-29A>G
ENST00000237623.11:c.499-29A>G	ENSP00000237623.7:n.499-29A>G
ENST00000360804.4:c.460-29A>G	ENSP00000354042.4:n.460-29A>G
ENST00000395080.7:c.541-29A>G	ENSP00000378517.3:n.541-29A>G
ENST00000508233.5:c.418-29A>G	ENSP00000422973.1:n.418-29A>G
ENST00000509659.5:n.830-29A>G
ENST00000614857.4:c.475-29A>G	ENSP00000477824.1:n.475-29A>G
NM_000582.2:c.499-29A>G	NP_000573.1:n.499-29A>G
NM_001040058.1:c.541-29A>G	NP_001035147.1:n.541-29A>G
NM_001040060.1:c.460-29A>G	NP_001035149.1:n.460-29A>G
NM_001251829.1:c.418-29A>G	NP_001238758.1:n.418-29A>G
NM_001251830.1:c.580-29A>G	NP_001238759.1:n.580-29A>G
NM_001040058.2:c.541-29A>G MANE Select	NP_001035147.1:n.541-29A>G
NM_000582.3:c.499-29A>G	NP_000573.1:n.499-29A>G
NM_001040060.2:c.460-29A>G	NP_001035149.1:n.460-29A>G
NM_001251829.2:c.418-29A>G	NP_001238758.1:n.418-29A>G
NM_001251830.2:c.580-29A>G	NP_001238759.1:n.580-29A>G