Canonical Allele Identifier: CA1474550851

Gene: SPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87981993_87981998delinsCTAGAT , CM000666.2:g.87981993_87981998delinsCTAGAT	GRCh38
NC_000004.11:g.88903145_88903150delinsCTAGAT , CM000666.1:g.88903145_88903150delinsCTAGAT	GRCh37
NC_000004.10:g.89122169_89122174delinsCTAGAT	NCBI36
NG_030362.1:g.11344_11349delinsCTAGAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000508233.6:c.417+195_417+200delinsCTAGAT	ENSP00000422973.2:n.417+195_417+200delins...
ENST00000614857.5:c.540+195_540+200delinsCTAGAT	ENSP00000477824.2:n.540+195_540+200delins...
ENST00000681973.1:n.767+195_767+200delinsCTAGAT
ENST00000682026.1:n.493+195_493+200delinsCTAGAT
ENST00000682448.1:n.2026+195_2026+200delinsCTAGAT
ENST00000682554.1:n.1988+195_1988+200delinsCTAGAT
ENST00000682599.1:n.3028+195_3028+200delinsCTAGAT
ENST00000682627.1:n.460+195_460+200delinsCTAGAT
ENST00000682865.1:n.824+195_824+200delinsCTAGAT
ENST00000683087.1:n.554+195_554+200delinsCTAGAT
ENST00000683168.1:n.1294+195_1294+200delinsCTAGAT
ENST00000683620.1:n.1722+195_1722+200delinsCTAGAT
ENST00000684106.1:n.2790+195_2790+200delinsCTAGAT
ENST00000684450.1:n.1599+195_1599+200delinsCTAGAT
ENST00000684710.1:n.1831+195_1831+200delinsCTAGAT
ENST00000395080.8:c.540+195_540+200delinsCTAGAT MANE Select	ENSP00000378517.3:n.540+195_540+200delins...
ENST00000237623.11:c.498+195_498+200delinsCTAGAT	ENSP00000237623.7:n.498+195_498+200delins...
ENST00000360804.4:c.459+195_459+200delinsCTAGAT	ENSP00000354042.4:n.459+195_459+200delins...
ENST00000395080.7:c.540+195_540+200delinsCTAGAT	ENSP00000378517.3:n.540+195_540+200delins...
ENST00000508233.5:c.417+195_417+200delinsCTAGAT	ENSP00000422973.1:n.417+195_417+200delins...
ENST00000509659.5:n.829+195_829+200delinsCTAGAT
ENST00000614857.4:c.474+195_474+200delinsCTAGAT	ENSP00000477824.1:n.474+195_474+200delins...
NM_000582.2:c.498+195_498+200delinsCTAGAT	NP_000573.1:n.498+195_498+200delinsCTAGAT...
NM_001040058.1:c.540+195_540+200delinsCTAGAT	NP_001035147.1:n.540+195_540+200delinsCTA...
NM_001040060.1:c.459+195_459+200delinsCTAGAT	NP_001035149.1:n.459+195_459+200delinsCTA...
NM_001251829.1:c.417+195_417+200delinsCTAGAT	NP_001238758.1:n.417+195_417+200delinsCTA...
NM_001251830.1:c.579+195_579+200delinsCTAGAT	NP_001238759.1:n.579+195_579+200delinsCTA...
NM_001040058.2:c.540+195_540+200delinsCTAGAT MANE Select	NP_001035147.1:n.540+195_540+200delinsCTA...
NM_000582.3:c.498+195_498+200delinsCTAGAT	NP_000573.1:n.498+195_498+200delinsCTAGAT...
NM_001040060.2:c.459+195_459+200delinsCTAGAT	NP_001035149.1:n.459+195_459+200delinsCTA...
NM_001251829.2:c.417+195_417+200delinsCTAGAT	NP_001238758.1:n.417+195_417+200delinsCTA...
NM_001251830.2:c.579+195_579+200delinsCTAGAT	NP_001238759.1:n.579+195_579+200delinsCTA...