Canonical Allele Identifier: CA100858094

Gene: SPP1

Linked Data

• dbSNP Id: rs1023092691
• gnomAD v3: 4-87982233-T-A
• gnomAD v4: 4-87982233-T-A
• MyVariant Identifiers: chr4:g.88903385T>A (hg19) ; chr4:g.87982233T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982233T>A , CM000666.2:g.87982233T>A	GRCh38
NC_000004.11:g.88903385T>A , CM000666.1:g.88903385T>A	GRCh37
NC_000004.10:g.89122409T>A	NCBI36
NG_030362.1:g.11584T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.418-259T>A	ENSP00000422973.2:n.418-259T>A
ENST00000614857.5:c.541-259T>A	ENSP00000477824.2:n.541-259T>A
ENST00000681973.1:n.768-259T>A
ENST00000682026.1:n.494-259T>A
ENST00000682448.1:n.2027-259T>A
ENST00000682554.1:n.1989-259T>A
ENST00000682599.1:n.3029-259T>A
ENST00000682627.1:n.461-259T>A
ENST00000682865.1:n.825-259T>A
ENST00000683087.1:n.555-259T>A
ENST00000683168.1:n.1295-259T>A
ENST00000683620.1:n.1723-259T>A
ENST00000684106.1:n.2791-259T>A
ENST00000684450.1:n.1600-259T>A
ENST00000684710.1:n.1832-259T>A
ENST00000395080.8:c.541-259T>A MANE Select	ENSP00000378517.3:n.541-259T>A
ENST00000237623.11:c.499-259T>A	ENSP00000237623.7:n.499-259T>A
ENST00000360804.4:c.460-259T>A	ENSP00000354042.4:n.460-259T>A
ENST00000395080.7:c.541-259T>A	ENSP00000378517.3:n.541-259T>A
ENST00000508233.5:c.418-259T>A	ENSP00000422973.1:n.418-259T>A
ENST00000509659.5:n.830-259T>A
ENST00000614857.4:c.475-259T>A	ENSP00000477824.1:n.475-259T>A
NM_000582.2:c.499-259T>A	NP_000573.1:n.499-259T>A
NM_001040058.1:c.541-259T>A	NP_001035147.1:n.541-259T>A
NM_001040060.1:c.460-259T>A	NP_001035149.1:n.460-259T>A
NM_001251829.1:c.418-259T>A	NP_001238758.1:n.418-259T>A
NM_001251830.1:c.580-259T>A	NP_001238759.1:n.580-259T>A
NM_001040058.2:c.541-259T>A MANE Select	NP_001035147.1:n.541-259T>A
NM_000582.3:c.499-259T>A	NP_000573.1:n.499-259T>A
NM_001040060.2:c.460-259T>A	NP_001035149.1:n.460-259T>A
NM_001251829.2:c.418-259T>A	NP_001238758.1:n.418-259T>A
NM_001251830.2:c.580-259T>A	NP_001238759.1:n.580-259T>A