Canonical Allele Identifier: CA357618237

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903664G>C (hg19) ; chr4:g.87982512G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982512G>C , CM000666.2:g.87982512G>C	GRCh38
NC_000004.11:g.88903664G>C , CM000666.1:g.88903664G>C	GRCh37
NC_000004.10:g.89122688G>C	NCBI36
NG_030362.1:g.11863G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.438G>C	ENSP00000422973.2:p.Glu146Asp
ENST00000614857.5:c.561G>C	ENSP00000477824.2:p.Glu187Asp
ENST00000681973.1:n.788G>C
ENST00000682026.1:n.514G>C
ENST00000682448.1:n.2047G>C
ENST00000682554.1:n.2009G>C
ENST00000682599.1:n.3049G>C
ENST00000682627.1:n.481G>C
ENST00000682865.1:n.845G>C
ENST00000683087.1:n.575G>C
ENST00000683168.1:n.1315G>C
ENST00000683620.1:n.1743G>C
ENST00000684106.1:n.2811G>C
ENST00000684450.1:n.1620G>C
ENST00000684710.1:n.1852G>C
ENST00000395080.8:c.561G>C MANE Select	ENSP00000378517.3:p.Glu187Asp
ENST00000237623.11:c.519G>C	ENSP00000237623.7:p.Glu173Asp
ENST00000360804.4:c.480G>C	ENSP00000354042.4:p.Glu160Asp
ENST00000395080.7:c.561G>C	ENSP00000378517.3:p.Glu187Asp
ENST00000508233.5:c.438G>C	ENSP00000422973.1:p.Glu146Asp
ENST00000509659.5:n.850G>C
ENST00000614857.4:c.495G>C	ENSP00000477824.1:p.Glu165Asp
NM_000582.2:c.519G>C	NP_000573.1:p.Glu173Asp
NM_001040058.1:c.561G>C	NP_001035147.1:p.Glu187Asp
NM_001040060.1:c.480G>C	NP_001035149.1:p.Glu160Asp
NM_001251829.1:c.438G>C	NP_001238758.1:p.Glu146Asp
NM_001251830.1:c.600G>C	NP_001238759.1:p.Glu200Asp
NM_001040058.2:c.561G>C MANE Select	NP_001035147.1:p.Glu187Asp
NM_000582.3:c.519G>C	NP_000573.1:p.Glu173Asp
NM_001040060.2:c.480G>C	NP_001035149.1:p.Glu160Asp
NM_001251829.2:c.438G>C	NP_001238758.1:p.Glu146Asp
NM_001251830.2:c.600G>C	NP_001238759.1:p.Glu200Asp