Canonical Allele Identifier: CA357618272

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903671A>T (hg19) ; chr4:g.87982519A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982519A>T , CM000666.2:g.87982519A>T	GRCh38
NC_000004.11:g.88903671A>T , CM000666.1:g.88903671A>T	GRCh37
NC_000004.10:g.89122695A>T	NCBI36
NG_030362.1:g.11870A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.445A>T	ENSP00000422973.2:p.Thr149Ser
ENST00000614857.5:c.568A>T	ENSP00000477824.2:p.Thr190Ser
ENST00000681973.1:n.795A>T
ENST00000682026.1:n.521A>T
ENST00000682448.1:n.2054A>T
ENST00000682554.1:n.2016A>T
ENST00000682599.1:n.3056A>T
ENST00000682627.1:n.488A>T
ENST00000682865.1:n.852A>T
ENST00000683087.1:n.582A>T
ENST00000683168.1:n.1322A>T
ENST00000683620.1:n.1750A>T
ENST00000684106.1:n.2818A>T
ENST00000684450.1:n.1627A>T
ENST00000684710.1:n.1859A>T
ENST00000395080.8:c.568A>T MANE Select	ENSP00000378517.3:p.Thr190Ser
ENST00000237623.11:c.526A>T	ENSP00000237623.7:p.Thr176Ser
ENST00000360804.4:c.487A>T	ENSP00000354042.4:p.Thr163Ser
ENST00000395080.7:c.568A>T	ENSP00000378517.3:p.Thr190Ser
ENST00000508233.5:c.445A>T	ENSP00000422973.1:p.Thr149Ser
ENST00000509659.5:n.857A>T
ENST00000614857.4:c.502A>T	ENSP00000477824.1:p.Thr168Ser
NM_000582.2:c.526A>T	NP_000573.1:p.Thr176Ser
NM_001040058.1:c.568A>T	NP_001035147.1:p.Thr190Ser
NM_001040060.1:c.487A>T	NP_001035149.1:p.Thr163Ser
NM_001251829.1:c.445A>T	NP_001238758.1:p.Thr149Ser
NM_001251830.1:c.607A>T	NP_001238759.1:p.Thr203Ser
NM_001040058.2:c.568A>T MANE Select	NP_001035147.1:p.Thr190Ser
NM_000582.3:c.526A>T	NP_000573.1:p.Thr176Ser
NM_001040060.2:c.487A>T	NP_001035149.1:p.Thr163Ser
NM_001251829.2:c.445A>T	NP_001238758.1:p.Thr149Ser
NM_001251830.2:c.607A>T	NP_001238759.1:p.Thr203Ser