Canonical Allele Identifier: CA357618255

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903668A>C (hg19) ; chr4:g.87982516A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982516A>C , CM000666.2:g.87982516A>C	GRCh38
NC_000004.11:g.88903668A>C , CM000666.1:g.88903668A>C	GRCh37
NC_000004.10:g.89122692A>C	NCBI36
NG_030362.1:g.11867A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.442A>C	ENSP00000422973.2:p.Ile148Leu
ENST00000614857.5:c.565A>C	ENSP00000477824.2:p.Ile189Leu
ENST00000681973.1:n.792A>C
ENST00000682026.1:n.518A>C
ENST00000682448.1:n.2051A>C
ENST00000682554.1:n.2013A>C
ENST00000682599.1:n.3053A>C
ENST00000682627.1:n.485A>C
ENST00000682865.1:n.849A>C
ENST00000683087.1:n.579A>C
ENST00000683168.1:n.1319A>C
ENST00000683620.1:n.1747A>C
ENST00000684106.1:n.2815A>C
ENST00000684450.1:n.1624A>C
ENST00000684710.1:n.1856A>C
ENST00000395080.8:c.565A>C MANE Select	ENSP00000378517.3:p.Ile189Leu
ENST00000237623.11:c.523A>C	ENSP00000237623.7:p.Ile175Leu
ENST00000360804.4:c.484A>C	ENSP00000354042.4:p.Ile162Leu
ENST00000395080.7:c.565A>C	ENSP00000378517.3:p.Ile189Leu
ENST00000508233.5:c.442A>C	ENSP00000422973.1:p.Ile148Leu
ENST00000509659.5:n.854A>C
ENST00000614857.4:c.499A>C	ENSP00000477824.1:p.Ile167Leu
NM_000582.2:c.523A>C	NP_000573.1:p.Ile175Leu
NM_001040058.1:c.565A>C	NP_001035147.1:p.Ile189Leu
NM_001040060.1:c.484A>C	NP_001035149.1:p.Ile162Leu
NM_001251829.1:c.442A>C	NP_001238758.1:p.Ile148Leu
NM_001251830.1:c.604A>C	NP_001238759.1:p.Ile202Leu
NM_001040058.2:c.565A>C MANE Select	NP_001035147.1:p.Ile189Leu
NM_000582.3:c.523A>C	NP_000573.1:p.Ile175Leu
NM_001040060.2:c.484A>C	NP_001035149.1:p.Ile162Leu
NM_001251829.2:c.442A>C	NP_001238758.1:p.Ile148Leu
NM_001251830.2:c.604A>C	NP_001238759.1:p.Ile202Leu