Canonical Allele Identifier: CA357618174

Gene: SPP1

Linked Data

• dbSNP Id: rs1725687680
• MyVariant Identifiers: chr4:g.88903648C>G (hg19) ; chr4:g.87982496C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982496C>G , CM000666.2:g.87982496C>G	GRCh38
NC_000004.11:g.88903648C>G , CM000666.1:g.88903648C>G	GRCh37
NC_000004.10:g.89122672C>G	NCBI36
NG_030362.1:g.11847C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.422C>G	ENSP00000422973.2:p.Pro141Arg
ENST00000614857.5:c.545C>G	ENSP00000477824.2:p.Pro182Arg
ENST00000681973.1:n.772C>G
ENST00000682026.1:n.498C>G
ENST00000682448.1:n.2031C>G
ENST00000682554.1:n.1993C>G
ENST00000682599.1:n.3033C>G
ENST00000682627.1:n.465C>G
ENST00000682865.1:n.829C>G
ENST00000683087.1:n.559C>G
ENST00000683168.1:n.1299C>G
ENST00000683620.1:n.1727C>G
ENST00000684106.1:n.2795C>G
ENST00000684450.1:n.1604C>G
ENST00000684710.1:n.1836C>G
ENST00000395080.8:c.545C>G MANE Select	ENSP00000378517.3:p.Pro182Arg
ENST00000237623.11:c.503C>G	ENSP00000237623.7:p.Pro168Arg
ENST00000360804.4:c.464C>G	ENSP00000354042.4:p.Pro155Arg
ENST00000395080.7:c.545C>G	ENSP00000378517.3:p.Pro182Arg
ENST00000508233.5:c.422C>G	ENSP00000422973.1:p.Pro141Arg
ENST00000509659.5:n.834C>G
ENST00000614857.4:c.479C>G	ENSP00000477824.1:p.Pro160Arg
NM_000582.2:c.503C>G	NP_000573.1:p.Pro168Arg
NM_001040058.1:c.545C>G	NP_001035147.1:p.Pro182Arg
NM_001040060.1:c.464C>G	NP_001035149.1:p.Pro155Arg
NM_001251829.1:c.422C>G	NP_001238758.1:p.Pro141Arg
NM_001251830.1:c.584C>G	NP_001238759.1:p.Pro195Arg
NM_001040058.2:c.545C>G MANE Select	NP_001035147.1:p.Pro182Arg
NM_000582.3:c.503C>G	NP_000573.1:p.Pro168Arg
NM_001040060.2:c.464C>G	NP_001035149.1:p.Pro155Arg
NM_001251829.2:c.422C>G	NP_001238758.1:p.Pro141Arg
NM_001251830.2:c.584C>G	NP_001238759.1:p.Pro195Arg