Canonical Allele Identifier: CA357618201

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903656A>G (hg19) ; chr4:g.87982504A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982504A>G , CM000666.2:g.87982504A>G	GRCh38
NC_000004.11:g.88903656A>G , CM000666.1:g.88903656A>G	GRCh37
NC_000004.10:g.89122680A>G	NCBI36
NG_030362.1:g.11855A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.430A>G	ENSP00000422973.2:p.Thr144Ala
ENST00000614857.5:c.553A>G	ENSP00000477824.2:p.Thr185Ala
ENST00000681973.1:n.780A>G
ENST00000682026.1:n.506A>G
ENST00000682448.1:n.2039A>G
ENST00000682554.1:n.2001A>G
ENST00000682599.1:n.3041A>G
ENST00000682627.1:n.473A>G
ENST00000682865.1:n.837A>G
ENST00000683087.1:n.567A>G
ENST00000683168.1:n.1307A>G
ENST00000683620.1:n.1735A>G
ENST00000684106.1:n.2803A>G
ENST00000684450.1:n.1612A>G
ENST00000684710.1:n.1844A>G
ENST00000395080.8:c.553A>G MANE Select	ENSP00000378517.3:p.Thr185Ala
ENST00000237623.11:c.511A>G	ENSP00000237623.7:p.Thr171Ala
ENST00000360804.4:c.472A>G	ENSP00000354042.4:p.Thr158Ala
ENST00000395080.7:c.553A>G	ENSP00000378517.3:p.Thr185Ala
ENST00000508233.5:c.430A>G	ENSP00000422973.1:p.Thr144Ala
ENST00000509659.5:n.842A>G
ENST00000614857.4:c.487A>G	ENSP00000477824.1:p.Thr163Ala
NM_000582.2:c.511A>G	NP_000573.1:p.Thr171Ala
NM_001040058.1:c.553A>G	NP_001035147.1:p.Thr185Ala
NM_001040060.1:c.472A>G	NP_001035149.1:p.Thr158Ala
NM_001251829.1:c.430A>G	NP_001238758.1:p.Thr144Ala
NM_001251830.1:c.592A>G	NP_001238759.1:p.Thr198Ala
NM_001040058.2:c.553A>G MANE Select	NP_001035147.1:p.Thr185Ala
NM_000582.3:c.511A>G	NP_000573.1:p.Thr171Ala
NM_001040060.2:c.472A>G	NP_001035149.1:p.Thr158Ala
NM_001251829.2:c.430A>G	NP_001238758.1:p.Thr144Ala
NM_001251830.2:c.592A>G	NP_001238759.1:p.Thr198Ala