Canonical Allele Identifier: CA440296398

Gene: SPP1

Linked Data

• MyVariant Identifiers: chr4:g.88903670C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982518C>T , CM000666.2:g.87982518C>T	GRCh38
NC_000004.11:g.88903670C>T , CM000666.1:g.88903670C>T	GRCh37
NC_000004.10:g.89122694C>T	NCBI36
NG_030362.1:g.11869C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.444C>T	ENSP00000422973.2:p.Ile148=
ENST00000614857.5:c.567C>T	ENSP00000477824.2:p.Ile189=
ENST00000681973.1:n.794C>T
ENST00000682026.1:n.520C>T
ENST00000682448.1:n.2053C>T
ENST00000682554.1:n.2015C>T
ENST00000682599.1:n.3055C>T
ENST00000682627.1:n.487C>T
ENST00000682865.1:n.851C>T
ENST00000683087.1:n.581C>T
ENST00000683168.1:n.1321C>T
ENST00000683620.1:n.1749C>T
ENST00000684106.1:n.2817C>T
ENST00000684450.1:n.1626C>T
ENST00000684710.1:n.1858C>T
ENST00000395080.8:c.567C>T MANE Select	ENSP00000378517.3:p.Ile189=
ENST00000237623.11:c.525C>T	ENSP00000237623.7:p.Ile175=
ENST00000360804.4:c.486C>T	ENSP00000354042.4:p.Ile162=
ENST00000395080.7:c.567C>T	ENSP00000378517.3:p.Ile189=
ENST00000508233.5:c.444C>T	ENSP00000422973.1:p.Ile148=
ENST00000509659.5:n.856C>T
ENST00000614857.4:c.501C>T	ENSP00000477824.1:p.Ile167=
NM_000582.2:c.525C>T	NP_000573.1:p.Ile175=
NM_001040058.1:c.567C>T	NP_001035147.1:p.Ile189=
NM_001040060.1:c.486C>T	NP_001035149.1:p.Ile162=
NM_001251829.1:c.444C>T	NP_001238758.1:p.Ile148=
NM_001251830.1:c.606C>T	NP_001238759.1:p.Ile202=
NM_001040058.2:c.567C>T MANE Select	NP_001035147.1:p.Ile189=
NM_000582.3:c.525C>T	NP_000573.1:p.Ile175=
NM_001040060.2:c.486C>T	NP_001035149.1:p.Ile162=
NM_001251829.2:c.444C>T	NP_001238758.1:p.Ile148=
NM_001251830.2:c.606C>T	NP_001238759.1:p.Ile202=