Canonical Allele Identifier: CA799617671

Gene: SPP1

Linked Data

• dbSNP Id: rs1199254414
• MyVariant Identifiers: chr4:g.88903117G>A (hg19) ; chr4:g.87981965G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87981965G>A , CM000666.2:g.87981965G>A	GRCh38
NC_000004.11:g.88903117G>A , CM000666.1:g.88903117G>A	GRCh37
NC_000004.10:g.89122141G>A	NCBI36
NG_030362.1:g.11316G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000508233.6:c.417+167G>A	ENSP00000422973.2:n.417+167G>A
ENST00000614857.5:c.540+167G>A	ENSP00000477824.2:n.540+167G>A
ENST00000681973.1:n.767+167G>A
ENST00000682026.1:n.493+167G>A
ENST00000682448.1:n.2026+167G>A
ENST00000682554.1:n.1988+167G>A
ENST00000682599.1:n.3028+167G>A
ENST00000682627.1:n.460+167G>A
ENST00000682655.1:c.*128G>A	ENSP00000508280.1:n.*128G>A
ENST00000682865.1:n.824+167G>A
ENST00000683087.1:n.554+167G>A
ENST00000683168.1:n.1294+167G>A
ENST00000683620.1:n.1722+167G>A
ENST00000684106.1:n.2790+167G>A
ENST00000684450.1:n.1599+167G>A
ENST00000684710.1:n.1831+167G>A
ENST00000395080.8:c.540+167G>A MANE Select	ENSP00000378517.3:n.540+167G>A
ENST00000237623.11:c.498+167G>A	ENSP00000237623.7:n.498+167G>A
ENST00000360804.4:c.459+167G>A	ENSP00000354042.4:n.459+167G>A
ENST00000395080.7:c.540+167G>A	ENSP00000378517.3:n.540+167G>A
ENST00000508233.5:c.417+167G>A	ENSP00000422973.1:n.417+167G>A
ENST00000509659.5:n.829+167G>A
ENST00000614857.4:c.474+167G>A	ENSP00000477824.1:n.474+167G>A
NM_000582.2:c.498+167G>A	NP_000573.1:n.498+167G>A
NM_001040058.1:c.540+167G>A	NP_001035147.1:n.540+167G>A
NM_001040060.1:c.459+167G>A	NP_001035149.1:n.459+167G>A
NM_001251829.1:c.417+167G>A	NP_001238758.1:n.417+167G>A
NM_001251830.1:c.579+167G>A	NP_001238759.1:n.579+167G>A
NM_001040058.2:c.540+167G>A MANE Select	NP_001035147.1:n.540+167G>A
NM_000582.3:c.498+167G>A	NP_000573.1:n.498+167G>A
NM_001040060.2:c.459+167G>A	NP_001035149.1:n.459+167G>A
NM_001251829.2:c.417+167G>A	NP_001238758.1:n.417+167G>A
NM_001251830.2:c.579+167G>A	NP_001238759.1:n.579+167G>A