Canonical Allele Identifier: CA3003452

Gene: SPP1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87977789C>T , CM000666.2:g.87977789C>T	GRCh38
NC_000004.11:g.88898941C>T , CM000666.1:g.88898941C>T	GRCh37
NC_000004.10:g.89117965C>T	NCBI36
NG_030362.1:g.7140C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.93+692C>T	ENSP00000422973.2:n.93+692C>T
ENST00000614857.5:c.93+692C>T	ENSP00000477824.2:n.93+692C>T
ENST00000681973.1:n.320+2C>T
ENST00000682554.1:n.1275+692C>T
ENST00000682599.1:n.1275+692C>T
ENST00000682627.1:n.94+692C>T
ENST00000682655.1:c.93+692C>T	ENSP00000508280.1:n.93+692C>T
ENST00000682865.1:n.500+692C>T
ENST00000683087.1:n.149+692C>T
ENST00000683440.1:n.1987C>T
ENST00000683620.1:n.1275+692C>T
ENST00000684106.1:n.1384+692C>T
ENST00000684450.1:n.1275+692C>T
ENST00000684710.1:n.1384+692C>T
ENST00000395080.8:c.93+692C>T MANE Select	ENSP00000378517.3:n.93+692C>T
ENST00000237623.11:c.93+692C>T	ENSP00000237623.7:n.93+692C>T
ENST00000360804.4:c.93+692C>T	ENSP00000354042.4:n.93+692C>T
ENST00000395080.7:c.93+692C>T	ENSP00000378517.3:n.93+692C>T
ENST00000504310.5:n.322C>T
ENST00000505146.1:n.109+692C>T
ENST00000508002.5:n.191+692C>T
ENST00000508233.5:c.93+692C>T	ENSP00000422973.1:n.93+692C>T
ENST00000509334.5:n.322C>T
ENST00000509659.5:n.321C>T
ENST00000513981.5:n.322C>T
ENST00000614857.4:c.93+692C>T	ENSP00000477824.1:n.93+692C>T
NM_000582.2:c.93+692C>T	NP_000573.1:n.93+692C>T
NM_001040058.1:c.93+692C>T	NP_001035147.1:n.93+692C>T
NM_001040060.1:c.93+692C>T	NP_001035149.1:n.93+692C>T
NM_001251829.1:c.93+692C>T	NP_001238758.1:n.93+692C>T
NM_001251830.1:c.71C>T	NP_001238759.1:p.Ala24Val
NM_001040058.2:c.93+692C>T MANE Select	NP_001035147.1:n.93+692C>T
NM_000582.3:c.93+692C>T	NP_000573.1:n.93+692C>T
NM_001040060.2:c.93+692C>T	NP_001035149.1:n.93+692C>T
NM_001251829.2:c.93+692C>T	NP_001238758.1:n.93+692C>T
NM_001251830.2:c.71C>T	NP_001238759.1:p.Ala24Val