Canonical Allele Identifier: CA357618249

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903666A>T (hg19) ; chr4:g.87982514A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982514A>T , CM000666.2:g.87982514A>T	GRCh38
NC_000004.11:g.88903666A>T , CM000666.1:g.88903666A>T	GRCh37
NC_000004.10:g.89122690A>T	NCBI36
NG_030362.1:g.11865A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.440A>T	ENSP00000422973.2:p.Asp147Val
ENST00000614857.5:c.563A>T	ENSP00000477824.2:p.Asp188Val
ENST00000681973.1:n.790A>T
ENST00000682026.1:n.516A>T
ENST00000682448.1:n.2049A>T
ENST00000682554.1:n.2011A>T
ENST00000682599.1:n.3051A>T
ENST00000682627.1:n.483A>T
ENST00000682865.1:n.847A>T
ENST00000683087.1:n.577A>T
ENST00000683168.1:n.1317A>T
ENST00000683620.1:n.1745A>T
ENST00000684106.1:n.2813A>T
ENST00000684450.1:n.1622A>T
ENST00000684710.1:n.1854A>T
ENST00000395080.8:c.563A>T MANE Select	ENSP00000378517.3:p.Asp188Val
ENST00000237623.11:c.521A>T	ENSP00000237623.7:p.Asp174Val
ENST00000360804.4:c.482A>T	ENSP00000354042.4:p.Asp161Val
ENST00000395080.7:c.563A>T	ENSP00000378517.3:p.Asp188Val
ENST00000508233.5:c.440A>T	ENSP00000422973.1:p.Asp147Val
ENST00000509659.5:n.852A>T
ENST00000614857.4:c.497A>T	ENSP00000477824.1:p.Asp166Val
NM_000582.2:c.521A>T	NP_000573.1:p.Asp174Val
NM_001040058.1:c.563A>T	NP_001035147.1:p.Asp188Val
NM_001040060.1:c.482A>T	NP_001035149.1:p.Asp161Val
NM_001251829.1:c.440A>T	NP_001238758.1:p.Asp147Val
NM_001251830.1:c.602A>T	NP_001238759.1:p.Asp201Val
NM_001040058.2:c.563A>T MANE Select	NP_001035147.1:p.Asp188Val
NM_000582.3:c.521A>T	NP_000573.1:p.Asp174Val
NM_001040060.2:c.482A>T	NP_001035149.1:p.Asp161Val
NM_001251829.2:c.440A>T	NP_001238758.1:p.Asp147Val
NM_001251830.2:c.602A>T	NP_001238759.1:p.Asp201Val