Canonical Allele Identifier: CA799617695

Gene: SPP1

Linked Data

• dbSNP Id: rs1350826889
• MyVariant Identifiers: chr4:g.88903141C>A (hg19) ; chr4:g.87981989C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87981989C>A , CM000666.2:g.87981989C>A	GRCh38
NC_000004.11:g.88903141C>A , CM000666.1:g.88903141C>A	GRCh37
NC_000004.10:g.89122165C>A	NCBI36
NG_030362.1:g.11340C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000508233.6:c.417+191C>A	ENSP00000422973.2:n.417+191C>A
ENST00000614857.5:c.540+191C>A	ENSP00000477824.2:n.540+191C>A
ENST00000681973.1:n.767+191C>A
ENST00000682026.1:n.493+191C>A
ENST00000682448.1:n.2026+191C>A
ENST00000682554.1:n.1988+191C>A
ENST00000682599.1:n.3028+191C>A
ENST00000682627.1:n.460+191C>A
ENST00000682655.1:c.*152C>A	ENSP00000508280.1:n.*152C>A
ENST00000682865.1:n.824+191C>A
ENST00000683087.1:n.554+191C>A
ENST00000683168.1:n.1294+191C>A
ENST00000683620.1:n.1722+191C>A
ENST00000684106.1:n.2790+191C>A
ENST00000684450.1:n.1599+191C>A
ENST00000684710.1:n.1831+191C>A
ENST00000395080.8:c.540+191C>A MANE Select	ENSP00000378517.3:n.540+191C>A
ENST00000237623.11:c.498+191C>A	ENSP00000237623.7:n.498+191C>A
ENST00000360804.4:c.459+191C>A	ENSP00000354042.4:n.459+191C>A
ENST00000395080.7:c.540+191C>A	ENSP00000378517.3:n.540+191C>A
ENST00000508233.5:c.417+191C>A	ENSP00000422973.1:n.417+191C>A
ENST00000509659.5:n.829+191C>A
ENST00000614857.4:c.474+191C>A	ENSP00000477824.1:n.474+191C>A
NM_000582.2:c.498+191C>A	NP_000573.1:n.498+191C>A
NM_001040058.1:c.540+191C>A	NP_001035147.1:n.540+191C>A
NM_001040060.1:c.459+191C>A	NP_001035149.1:n.459+191C>A
NM_001251829.1:c.417+191C>A	NP_001238758.1:n.417+191C>A
NM_001251830.1:c.579+191C>A	NP_001238759.1:n.579+191C>A
NM_001040058.2:c.540+191C>A MANE Select	NP_001035147.1:n.540+191C>A
NM_000582.3:c.498+191C>A	NP_000573.1:n.498+191C>A
NM_001040060.2:c.459+191C>A	NP_001035149.1:n.459+191C>A
NM_001251829.2:c.417+191C>A	NP_001238758.1:n.417+191C>A
NM_001251830.2:c.579+191C>A	NP_001238759.1:n.579+191C>A