Canonical Allele Identifier: CA3003621

Gene: SPP1

Linked Data

• dbSNP Id: rs767926035
• ExAC: 4:88903679 C / T
• gnomAD v2: 4-88903679-C-T
• gnomAD v4: 4-87982527-C-T
• MyVariant Identifiers: chr4:g.88903679C>T (hg19) ; chr4:g.87982527C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982527C>T , CM000666.2:g.87982527C>T	GRCh38
NC_000004.11:g.88903679C>T , CM000666.1:g.88903679C>T	GRCh37
NC_000004.10:g.89122703C>T	NCBI36
NG_030362.1:g.11878C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.453C>T	ENSP00000422973.2:p.His151=
ENST00000614857.5:c.576C>T	ENSP00000477824.2:p.His192=
ENST00000681973.1:n.803C>T
ENST00000682026.1:n.529C>T
ENST00000682448.1:n.2062C>T
ENST00000682554.1:n.2024C>T
ENST00000682599.1:n.3064C>T
ENST00000682627.1:n.496C>T
ENST00000682865.1:n.860C>T
ENST00000683087.1:n.590C>T
ENST00000683168.1:n.1330C>T
ENST00000683620.1:n.1758C>T
ENST00000684106.1:n.2826C>T
ENST00000684450.1:n.1635C>T
ENST00000684710.1:n.1867C>T
ENST00000395080.8:c.576C>T MANE Select	ENSP00000378517.3:p.His192=
ENST00000237623.11:c.534C>T	ENSP00000237623.7:p.His178=
ENST00000360804.4:c.495C>T	ENSP00000354042.4:p.His165=
ENST00000395080.7:c.576C>T	ENSP00000378517.3:p.His192=
ENST00000508233.5:c.453C>T	ENSP00000422973.1:p.His151=
ENST00000509659.5:n.865C>T
ENST00000614857.4:c.510C>T	ENSP00000477824.1:p.His170=
NM_000582.2:c.534C>T	NP_000573.1:p.His178=
NM_001040058.1:c.576C>T	NP_001035147.1:p.His192=
NM_001040060.1:c.495C>T	NP_001035149.1:p.His165=
NM_001251829.1:c.453C>T	NP_001238758.1:p.His151=
NM_001251830.1:c.615C>T	NP_001238759.1:p.His205=
NM_001040058.2:c.576C>T MANE Select	NP_001035147.1:p.His192=
NM_000582.3:c.534C>T	NP_000573.1:p.His178=
NM_001040060.2:c.495C>T	NP_001035149.1:p.His165=
NM_001251829.2:c.453C>T	NP_001238758.1:p.His151=
NM_001251830.2:c.615C>T	NP_001238759.1:p.His205=