Canonical Allele Identifier: CA2762535770

Gene: SPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982049C>T , CM000666.2:g.87982049C>T	GRCh38
NC_000004.11:g.88903201C>T , CM000666.1:g.88903201C>T	GRCh37
NC_000004.10:g.89122225C>T	NCBI36
NG_030362.1:g.11400C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.417+251C>T	ENSP00000422973.2:n.417+251C>T
ENST00000614857.5:c.540+251C>T	ENSP00000477824.2:n.540+251C>T
ENST00000681973.1:n.767+251C>T
ENST00000682026.1:n.493+251C>T
ENST00000682448.1:n.2026+251C>T
ENST00000682554.1:n.1988+251C>T
ENST00000682599.1:n.3028+251C>T
ENST00000682627.1:n.460+251C>T
ENST00000682865.1:n.824+251C>T
ENST00000683087.1:n.554+251C>T
ENST00000683168.1:n.1294+251C>T
ENST00000683620.1:n.1722+251C>T
ENST00000684106.1:n.2790+251C>T
ENST00000684450.1:n.1599+251C>T
ENST00000684710.1:n.1831+251C>T
ENST00000395080.8:c.540+251C>T MANE Select	ENSP00000378517.3:n.540+251C>T
ENST00000237623.11:c.498+251C>T	ENSP00000237623.7:n.498+251C>T
ENST00000360804.4:c.459+251C>T	ENSP00000354042.4:n.459+251C>T
ENST00000395080.7:c.540+251C>T	ENSP00000378517.3:n.540+251C>T
ENST00000508233.5:c.417+251C>T	ENSP00000422973.1:n.417+251C>T
ENST00000509659.5:n.829+251C>T
ENST00000614857.4:c.474+251C>T	ENSP00000477824.1:n.474+251C>T
NM_000582.2:c.498+251C>T	NP_000573.1:n.498+251C>T
NM_001040058.1:c.540+251C>T	NP_001035147.1:n.540+251C>T
NM_001040060.1:c.459+251C>T	NP_001035149.1:n.459+251C>T
NM_001251829.1:c.417+251C>T	NP_001238758.1:n.417+251C>T
NM_001251830.1:c.579+251C>T	NP_001238759.1:n.579+251C>T
NM_001040058.2:c.540+251C>T MANE Select	NP_001035147.1:n.540+251C>T
NM_000582.3:c.498+251C>T	NP_000573.1:n.498+251C>T
NM_001040060.2:c.459+251C>T	NP_001035149.1:n.459+251C>T
NM_001251829.2:c.417+251C>T	NP_001238758.1:n.417+251C>T
NM_001251830.2:c.579+251C>T	NP_001238759.1:n.579+251C>T