Canonical Allele Identifier: CA3003620

Gene: SPP1

Linked Data

• dbSNP Id: rs762490095
• ExAC: 4:88903669 T / A
• gnomAD v2: 4-88903669-T-A
• gnomAD v3: 4-87982517-T-A
• gnomAD v4: 4-87982517-T-A
• MyVariant Identifiers: chr4:g.88903669T>A (hg19) ; chr4:g.87982517T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982517T>A , CM000666.2:g.87982517T>A	GRCh38
NC_000004.11:g.88903669T>A , CM000666.1:g.88903669T>A	GRCh37
NC_000004.10:g.89122693T>A	NCBI36
NG_030362.1:g.11868T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.443T>A	ENSP00000422973.2:p.Ile148Asn
ENST00000614857.5:c.566T>A	ENSP00000477824.2:p.Ile189Asn
ENST00000681973.1:n.793T>A
ENST00000682026.1:n.519T>A
ENST00000682448.1:n.2052T>A
ENST00000682554.1:n.2014T>A
ENST00000682599.1:n.3054T>A
ENST00000682627.1:n.486T>A
ENST00000682865.1:n.850T>A
ENST00000683087.1:n.580T>A
ENST00000683168.1:n.1320T>A
ENST00000683620.1:n.1748T>A
ENST00000684106.1:n.2816T>A
ENST00000684450.1:n.1625T>A
ENST00000684710.1:n.1857T>A
ENST00000395080.8:c.566T>A MANE Select	ENSP00000378517.3:p.Ile189Asn
ENST00000237623.11:c.524T>A	ENSP00000237623.7:p.Ile175Asn
ENST00000360804.4:c.485T>A	ENSP00000354042.4:p.Ile162Asn
ENST00000395080.7:c.566T>A	ENSP00000378517.3:p.Ile189Asn
ENST00000508233.5:c.443T>A	ENSP00000422973.1:p.Ile148Asn
ENST00000509659.5:n.855T>A
ENST00000614857.4:c.500T>A	ENSP00000477824.1:p.Ile167Asn
NM_000582.2:c.524T>A	NP_000573.1:p.Ile175Asn
NM_001040058.1:c.566T>A	NP_001035147.1:p.Ile189Asn
NM_001040060.1:c.485T>A	NP_001035149.1:p.Ile162Asn
NM_001251829.1:c.443T>A	NP_001238758.1:p.Ile148Asn
NM_001251830.1:c.605T>A	NP_001238759.1:p.Ile202Asn
NM_001040058.2:c.566T>A MANE Select	NP_001035147.1:p.Ile189Asn
NM_000582.3:c.524T>A	NP_000573.1:p.Ile175Asn
NM_001040060.2:c.485T>A	NP_001035149.1:p.Ile162Asn
NM_001251829.2:c.443T>A	NP_001238758.1:p.Ile148Asn
NM_001251830.2:c.605T>A	NP_001238759.1:p.Ile202Asn