Canonical Allele Identifier: CA357618207

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903657C>G (hg19) ; chr4:g.87982505C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982505C>G , CM000666.2:g.87982505C>G	GRCh38
NC_000004.11:g.88903657C>G , CM000666.1:g.88903657C>G	GRCh37
NC_000004.10:g.89122681C>G	NCBI36
NG_030362.1:g.11856C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.431C>G	ENSP00000422973.2:p.Thr144Arg
ENST00000614857.5:c.554C>G	ENSP00000477824.2:p.Thr185Arg
ENST00000681973.1:n.781C>G
ENST00000682026.1:n.507C>G
ENST00000682448.1:n.2040C>G
ENST00000682554.1:n.2002C>G
ENST00000682599.1:n.3042C>G
ENST00000682627.1:n.474C>G
ENST00000682865.1:n.838C>G
ENST00000683087.1:n.568C>G
ENST00000683168.1:n.1308C>G
ENST00000683620.1:n.1736C>G
ENST00000684106.1:n.2804C>G
ENST00000684450.1:n.1613C>G
ENST00000684710.1:n.1845C>G
ENST00000395080.8:c.554C>G MANE Select	ENSP00000378517.3:p.Thr185Arg
ENST00000237623.11:c.512C>G	ENSP00000237623.7:p.Thr171Arg
ENST00000360804.4:c.473C>G	ENSP00000354042.4:p.Thr158Arg
ENST00000395080.7:c.554C>G	ENSP00000378517.3:p.Thr185Arg
ENST00000508233.5:c.431C>G	ENSP00000422973.1:p.Thr144Arg
ENST00000509659.5:n.843C>G
ENST00000614857.4:c.488C>G	ENSP00000477824.1:p.Thr163Arg
NM_000582.2:c.512C>G	NP_000573.1:p.Thr171Arg
NM_001040058.1:c.554C>G	NP_001035147.1:p.Thr185Arg
NM_001040060.1:c.473C>G	NP_001035149.1:p.Thr158Arg
NM_001251829.1:c.431C>G	NP_001238758.1:p.Thr144Arg
NM_001251830.1:c.593C>G	NP_001238759.1:p.Thr198Arg
NM_001040058.2:c.554C>G MANE Select	NP_001035147.1:p.Thr185Arg
NM_000582.3:c.512C>G	NP_000573.1:p.Thr171Arg
NM_001040060.2:c.473C>G	NP_001035149.1:p.Thr158Arg
NM_001251829.2:c.431C>G	NP_001238758.1:p.Thr144Arg
NM_001251830.2:c.593C>G	NP_001238759.1:p.Thr198Arg