Canonical Allele Identifier: CA357618200

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903656A>C (hg19) ; chr4:g.87982504A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982504A>C , CM000666.2:g.87982504A>C	GRCh38
NC_000004.11:g.88903656A>C , CM000666.1:g.88903656A>C	GRCh37
NC_000004.10:g.89122680A>C	NCBI36
NG_030362.1:g.11855A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.430A>C	ENSP00000422973.2:p.Thr144Pro
ENST00000614857.5:c.553A>C	ENSP00000477824.2:p.Thr185Pro
ENST00000681973.1:n.780A>C
ENST00000682026.1:n.506A>C
ENST00000682448.1:n.2039A>C
ENST00000682554.1:n.2001A>C
ENST00000682599.1:n.3041A>C
ENST00000682627.1:n.473A>C
ENST00000682865.1:n.837A>C
ENST00000683087.1:n.567A>C
ENST00000683168.1:n.1307A>C
ENST00000683620.1:n.1735A>C
ENST00000684106.1:n.2803A>C
ENST00000684450.1:n.1612A>C
ENST00000684710.1:n.1844A>C
ENST00000395080.8:c.553A>C MANE Select	ENSP00000378517.3:p.Thr185Pro
ENST00000237623.11:c.511A>C	ENSP00000237623.7:p.Thr171Pro
ENST00000360804.4:c.472A>C	ENSP00000354042.4:p.Thr158Pro
ENST00000395080.7:c.553A>C	ENSP00000378517.3:p.Thr185Pro
ENST00000508233.5:c.430A>C	ENSP00000422973.1:p.Thr144Pro
ENST00000509659.5:n.842A>C
ENST00000614857.4:c.487A>C	ENSP00000477824.1:p.Thr163Pro
NM_000582.2:c.511A>C	NP_000573.1:p.Thr171Pro
NM_001040058.1:c.553A>C	NP_001035147.1:p.Thr185Pro
NM_001040060.1:c.472A>C	NP_001035149.1:p.Thr158Pro
NM_001251829.1:c.430A>C	NP_001238758.1:p.Thr144Pro
NM_001251830.1:c.592A>C	NP_001238759.1:p.Thr198Pro
NM_001040058.2:c.553A>C MANE Select	NP_001035147.1:p.Thr185Pro
NM_000582.3:c.511A>C	NP_000573.1:p.Thr171Pro
NM_001040060.2:c.472A>C	NP_001035149.1:p.Thr158Pro
NM_001251829.2:c.430A>C	NP_001238758.1:p.Thr144Pro
NM_001251830.2:c.592A>C	NP_001238759.1:p.Thr198Pro