Canonical Allele Identifier: CA357618289

Gene: SPP1

Linked Data

• gnomAD v4: 4-87982525-C-T
• MyVariant Identifiers: chr4:g.88903677C>T (hg19) ; chr4:g.87982525C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982525C>T , CM000666.2:g.87982525C>T	GRCh38
NC_000004.11:g.88903677C>T , CM000666.1:g.88903677C>T	GRCh37
NC_000004.10:g.89122701C>T	NCBI36
NG_030362.1:g.11876C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.451C>T	ENSP00000422973.2:p.His151Tyr
ENST00000614857.5:c.574C>T	ENSP00000477824.2:p.His192Tyr
ENST00000681973.1:n.801C>T
ENST00000682026.1:n.527C>T
ENST00000682448.1:n.2060C>T
ENST00000682554.1:n.2022C>T
ENST00000682599.1:n.3062C>T
ENST00000682627.1:n.494C>T
ENST00000682865.1:n.858C>T
ENST00000683087.1:n.588C>T
ENST00000683168.1:n.1328C>T
ENST00000683620.1:n.1756C>T
ENST00000684106.1:n.2824C>T
ENST00000684450.1:n.1633C>T
ENST00000684710.1:n.1865C>T
ENST00000395080.8:c.574C>T MANE Select	ENSP00000378517.3:p.His192Tyr
ENST00000237623.11:c.532C>T	ENSP00000237623.7:p.His178Tyr
ENST00000360804.4:c.493C>T	ENSP00000354042.4:p.His165Tyr
ENST00000395080.7:c.574C>T	ENSP00000378517.3:p.His192Tyr
ENST00000508233.5:c.451C>T	ENSP00000422973.1:p.His151Tyr
ENST00000509659.5:n.863C>T
ENST00000614857.4:c.508C>T	ENSP00000477824.1:p.His170Tyr
NM_000582.2:c.532C>T	NP_000573.1:p.His178Tyr
NM_001040058.1:c.574C>T	NP_001035147.1:p.His192Tyr
NM_001040060.1:c.493C>T	NP_001035149.1:p.His165Tyr
NM_001251829.1:c.451C>T	NP_001238758.1:p.His151Tyr
NM_001251830.1:c.613C>T	NP_001238759.1:p.His205Tyr
NM_001040058.2:c.574C>T MANE Select	NP_001035147.1:p.His192Tyr
NM_000582.3:c.532C>T	NP_000573.1:p.His178Tyr
NM_001040060.2:c.493C>T	NP_001035149.1:p.His165Tyr
NM_001251829.2:c.451C>T	NP_001238758.1:p.His151Tyr
NM_001251830.2:c.613C>T	NP_001238759.1:p.His205Tyr