Canonical Allele Identifier: CA357618195

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903653G>C (hg19) ; chr4:g.87982501G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982501G>C , CM000666.2:g.87982501G>C	GRCh38
NC_000004.11:g.88903653G>C , CM000666.1:g.88903653G>C	GRCh37
NC_000004.10:g.89122677G>C	NCBI36
NG_030362.1:g.11852G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.427G>C	ENSP00000422973.2:p.Ala143Pro
ENST00000614857.5:c.550G>C	ENSP00000477824.2:p.Ala184Pro
ENST00000681973.1:n.777G>C
ENST00000682026.1:n.503G>C
ENST00000682448.1:n.2036G>C
ENST00000682554.1:n.1998G>C
ENST00000682599.1:n.3038G>C
ENST00000682627.1:n.470G>C
ENST00000682865.1:n.834G>C
ENST00000683087.1:n.564G>C
ENST00000683168.1:n.1304G>C
ENST00000683620.1:n.1732G>C
ENST00000684106.1:n.2800G>C
ENST00000684450.1:n.1609G>C
ENST00000684710.1:n.1841G>C
ENST00000395080.8:c.550G>C MANE Select	ENSP00000378517.3:p.Ala184Pro
ENST00000237623.11:c.508G>C	ENSP00000237623.7:p.Ala170Pro
ENST00000360804.4:c.469G>C	ENSP00000354042.4:p.Ala157Pro
ENST00000395080.7:c.550G>C	ENSP00000378517.3:p.Ala184Pro
ENST00000508233.5:c.427G>C	ENSP00000422973.1:p.Ala143Pro
ENST00000509659.5:n.839G>C
ENST00000614857.4:c.484G>C	ENSP00000477824.1:p.Ala162Pro
NM_000582.2:c.508G>C	NP_000573.1:p.Ala170Pro
NM_001040058.1:c.550G>C	NP_001035147.1:p.Ala184Pro
NM_001040060.1:c.469G>C	NP_001035149.1:p.Ala157Pro
NM_001251829.1:c.427G>C	NP_001238758.1:p.Ala143Pro
NM_001251830.1:c.589G>C	NP_001238759.1:p.Ala197Pro
NM_001040058.2:c.550G>C MANE Select	NP_001035147.1:p.Ala184Pro
NM_000582.3:c.508G>C	NP_000573.1:p.Ala170Pro
NM_001040060.2:c.469G>C	NP_001035149.1:p.Ala157Pro
NM_001251829.2:c.427G>C	NP_001238758.1:p.Ala143Pro
NM_001251830.2:c.589G>C	NP_001238759.1:p.Ala197Pro