Canonical Allele Identifier: CA3003531

Gene: SPP1

Linked Data

• dbSNP Id: rs4754
• ExAC: 4:88902692 T / C
• gnomAD v2: 4-88902692-T-C
• gnomAD v3: 4-87981540-T-C
• gnomAD v4: 4-87981540-T-C
• MyVariant Identifiers: chr4:g.88902692T>C (hg19) ; chr4:g.87981540T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87981540T>C , CM000666.2:g.87981540T>C	GRCh38
NC_000004.11:g.88902692T>C , CM000666.1:g.88902692T>C	GRCh37
NC_000004.10:g.89121716T>C	NCBI36
NG_030362.1:g.10891T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000508233.6:c.159T>C	ENSP00000422973.2:p.Asp53=
ENST00000614857.5:c.282T>C	ENSP00000477824.2:p.Asp94=
ENST00000681973.1:n.509T>C
ENST00000682026.1:n.235T>C
ENST00000682448.1:n.1768T>C
ENST00000682554.1:n.1730T>C
ENST00000682599.1:n.2770T>C
ENST00000682627.1:n.202T>C
ENST00000682655.1:c.282T>C	ENSP00000508280.1:p.Asp94=
ENST00000682865.1:n.566T>C
ENST00000683087.1:n.296T>C
ENST00000683168.1:n.1036T>C
ENST00000683620.1:n.1464T>C
ENST00000684106.1:n.2532T>C
ENST00000684450.1:n.1341T>C
ENST00000684710.1:n.1573T>C
ENST00000395080.8:c.282T>C MANE Select	ENSP00000378517.3:p.Asp94=
ENST00000237623.11:c.240T>C	ENSP00000237623.7:p.Asp80=
ENST00000360804.4:c.201T>C	ENSP00000354042.4:p.Asp67=
ENST00000395080.7:c.282T>C	ENSP00000378517.3:p.Asp94=
ENST00000508233.5:c.159T>C	ENSP00000422973.1:p.Asp53=
ENST00000509334.5:n.539T>C
ENST00000509659.5:n.571T>C
ENST00000513981.5:n.581T>C
ENST00000614857.4:c.277+5T>C	ENSP00000477824.1:n.277+5T>C
NM_000582.2:c.240T>C	NP_000573.1:p.Asp80=
NM_001040058.1:c.282T>C	NP_001035147.1:p.Asp94=
NM_001040060.1:c.201T>C	NP_001035149.1:p.Asp67=
NM_001251829.1:c.159T>C	NP_001238758.1:p.Asp53=
NM_001251830.1:c.321T>C	NP_001238759.1:p.Asp107=
NM_001040058.2:c.282T>C MANE Select	NP_001035147.1:p.Asp94=
NM_000582.3:c.240T>C	NP_000573.1:p.Asp80=
NM_001040060.2:c.201T>C	NP_001035149.1:p.Asp67=
NM_001251829.2:c.159T>C	NP_001238758.1:p.Asp53=
NM_001251830.2:c.321T>C	NP_001238759.1:p.Asp107=