Canonical Allele Identifier: CA357618263

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903669T>C (hg19) ; chr4:g.87982517T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982517T>C , CM000666.2:g.87982517T>C	GRCh38
NC_000004.11:g.88903669T>C , CM000666.1:g.88903669T>C	GRCh37
NC_000004.10:g.89122693T>C	NCBI36
NG_030362.1:g.11868T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.443T>C	ENSP00000422973.2:p.Ile148Thr
ENST00000614857.5:c.566T>C	ENSP00000477824.2:p.Ile189Thr
ENST00000681973.1:n.793T>C
ENST00000682026.1:n.519T>C
ENST00000682448.1:n.2052T>C
ENST00000682554.1:n.2014T>C
ENST00000682599.1:n.3054T>C
ENST00000682627.1:n.486T>C
ENST00000682865.1:n.850T>C
ENST00000683087.1:n.580T>C
ENST00000683168.1:n.1320T>C
ENST00000683620.1:n.1748T>C
ENST00000684106.1:n.2816T>C
ENST00000684450.1:n.1625T>C
ENST00000684710.1:n.1857T>C
ENST00000395080.8:c.566T>C MANE Select	ENSP00000378517.3:p.Ile189Thr
ENST00000237623.11:c.524T>C	ENSP00000237623.7:p.Ile175Thr
ENST00000360804.4:c.485T>C	ENSP00000354042.4:p.Ile162Thr
ENST00000395080.7:c.566T>C	ENSP00000378517.3:p.Ile189Thr
ENST00000508233.5:c.443T>C	ENSP00000422973.1:p.Ile148Thr
ENST00000509659.5:n.855T>C
ENST00000614857.4:c.500T>C	ENSP00000477824.1:p.Ile167Thr
NM_000582.2:c.524T>C	NP_000573.1:p.Ile175Thr
NM_001040058.1:c.566T>C	NP_001035147.1:p.Ile189Thr
NM_001040060.1:c.485T>C	NP_001035149.1:p.Ile162Thr
NM_001251829.1:c.443T>C	NP_001238758.1:p.Ile148Thr
NM_001251830.1:c.605T>C	NP_001238759.1:p.Ile202Thr
NM_001040058.2:c.566T>C MANE Select	NP_001035147.1:p.Ile189Thr
NM_000582.3:c.524T>C	NP_000573.1:p.Ile175Thr
NM_001040060.2:c.485T>C	NP_001035149.1:p.Ile162Thr
NM_001251829.2:c.443T>C	NP_001238758.1:p.Ile148Thr
NM_001251830.2:c.605T>C	NP_001238759.1:p.Ile202Thr