Canonical Allele Identifier: CA440296383

Gene: SPP1

Linked Data

• gnomAD v4: 4-87982494-C-T
• COSMIC: COSM5931552
• MyVariant Identifiers: chr4:g.88903646C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982494C>T , CM000666.2:g.87982494C>T	GRCh38
NC_000004.11:g.88903646C>T , CM000666.1:g.88903646C>T	GRCh37
NC_000004.10:g.89122670C>T	NCBI36
NG_030362.1:g.11845C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.420C>T	ENSP00000422973.2:p.Tyr140=
ENST00000614857.5:c.543C>T	ENSP00000477824.2:p.Tyr181=
ENST00000681973.1:n.770C>T
ENST00000682026.1:n.496C>T
ENST00000682448.1:n.2029C>T
ENST00000682554.1:n.1991C>T
ENST00000682599.1:n.3031C>T
ENST00000682627.1:n.463C>T
ENST00000682865.1:n.827C>T
ENST00000683087.1:n.557C>T
ENST00000683168.1:n.1297C>T
ENST00000683620.1:n.1725C>T
ENST00000684106.1:n.2793C>T
ENST00000684450.1:n.1602C>T
ENST00000684710.1:n.1834C>T
ENST00000395080.8:c.543C>T MANE Select	ENSP00000378517.3:p.Tyr181=
ENST00000237623.11:c.501C>T	ENSP00000237623.7:p.Tyr167=
ENST00000360804.4:c.462C>T	ENSP00000354042.4:p.Tyr154=
ENST00000395080.7:c.543C>T	ENSP00000378517.3:p.Tyr181=
ENST00000508233.5:c.420C>T	ENSP00000422973.1:p.Tyr140=
ENST00000509659.5:n.832C>T
ENST00000614857.4:c.477C>T	ENSP00000477824.1:p.Tyr159=
NM_000582.2:c.501C>T	NP_000573.1:p.Tyr167=
NM_001040058.1:c.543C>T	NP_001035147.1:p.Tyr181=
NM_001040060.1:c.462C>T	NP_001035149.1:p.Tyr154=
NM_001251829.1:c.420C>T	NP_001238758.1:p.Tyr140=
NM_001251830.1:c.582C>T	NP_001238759.1:p.Tyr194=
NM_001040058.2:c.543C>T MANE Select	NP_001035147.1:p.Tyr181=
NM_000582.3:c.501C>T	NP_000573.1:p.Tyr167=
NM_001040060.2:c.462C>T	NP_001035149.1:p.Tyr154=
NM_001251829.2:c.420C>T	NP_001238758.1:p.Tyr140=
NM_001251830.2:c.582C>T	NP_001238759.1:p.Tyr194=