Canonical Allele Identifier: CA440296385

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903649T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982497T>C , CM000666.2:g.87982497T>C	GRCh38
NC_000004.11:g.88903649T>C , CM000666.1:g.88903649T>C	GRCh37
NC_000004.10:g.89122673T>C	NCBI36
NG_030362.1:g.11848T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.423T>C	ENSP00000422973.2:p.Pro141=
ENST00000614857.5:c.546T>C	ENSP00000477824.2:p.Pro182=
ENST00000681973.1:n.773T>C
ENST00000682026.1:n.499T>C
ENST00000682448.1:n.2032T>C
ENST00000682554.1:n.1994T>C
ENST00000682599.1:n.3034T>C
ENST00000682627.1:n.466T>C
ENST00000682865.1:n.830T>C
ENST00000683087.1:n.560T>C
ENST00000683168.1:n.1300T>C
ENST00000683620.1:n.1728T>C
ENST00000684106.1:n.2796T>C
ENST00000684450.1:n.1605T>C
ENST00000684710.1:n.1837T>C
ENST00000395080.8:c.546T>C MANE Select	ENSP00000378517.3:p.Pro182=
ENST00000237623.11:c.504T>C	ENSP00000237623.7:p.Pro168=
ENST00000360804.4:c.465T>C	ENSP00000354042.4:p.Pro155=
ENST00000395080.7:c.546T>C	ENSP00000378517.3:p.Pro182=
ENST00000508233.5:c.423T>C	ENSP00000422973.1:p.Pro141=
ENST00000509659.5:n.835T>C
ENST00000614857.4:c.480T>C	ENSP00000477824.1:p.Pro160=
NM_000582.2:c.504T>C	NP_000573.1:p.Pro168=
NM_001040058.1:c.546T>C	NP_001035147.1:p.Pro182=
NM_001040060.1:c.465T>C	NP_001035149.1:p.Pro155=
NM_001251829.1:c.423T>C	NP_001238758.1:p.Pro141=
NM_001251830.1:c.585T>C	NP_001238759.1:p.Pro195=
NM_001040058.2:c.546T>C MANE Select	NP_001035147.1:p.Pro182=
NM_000582.3:c.504T>C	NP_000573.1:p.Pro168=
NM_001040060.2:c.465T>C	NP_001035149.1:p.Pro155=
NM_001251829.2:c.423T>C	NP_001238758.1:p.Pro141=
NM_001251830.2:c.585T>C	NP_001238759.1:p.Pro195=