Canonical Allele Identifier: CA552864115

Gene: SPP1

Linked Data

• dbSNP Id: rs1377557273
• gnomAD v2: 4-88903252-G-A
• gnomAD v3: 4-87982100-G-A
• gnomAD v4: 4-87982100-G-A
• MyVariant Identifiers: chr4:g.88903252G>A (hg19) ; chr4:g.87982100G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982100G>A , CM000666.2:g.87982100G>A	GRCh38
NC_000004.11:g.88903252G>A , CM000666.1:g.88903252G>A	GRCh37
NC_000004.10:g.89122276G>A	NCBI36
NG_030362.1:g.11451G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000508233.6:c.417+302G>A	ENSP00000422973.2:n.417+302G>A
ENST00000614857.5:c.540+302G>A	ENSP00000477824.2:n.540+302G>A
ENST00000681973.1:n.767+302G>A
ENST00000682026.1:n.493+302G>A
ENST00000682448.1:n.2026+302G>A
ENST00000682554.1:n.1988+302G>A
ENST00000682599.1:n.3028+302G>A
ENST00000682627.1:n.460+302G>A
ENST00000682865.1:n.824+302G>A
ENST00000683087.1:n.554+302G>A
ENST00000683168.1:n.1294+302G>A
ENST00000683620.1:n.1722+302G>A
ENST00000684106.1:n.2790+302G>A
ENST00000684450.1:n.1599+302G>A
ENST00000684710.1:n.1831+302G>A
ENST00000395080.8:c.540+302G>A MANE Select	ENSP00000378517.3:n.540+302G>A
ENST00000237623.11:c.498+302G>A	ENSP00000237623.7:n.498+302G>A
ENST00000360804.4:c.459+302G>A	ENSP00000354042.4:n.459+302G>A
ENST00000395080.7:c.540+302G>A	ENSP00000378517.3:n.540+302G>A
ENST00000508233.5:c.417+302G>A	ENSP00000422973.1:n.417+302G>A
ENST00000509659.5:n.829+302G>A
ENST00000614857.4:c.474+302G>A	ENSP00000477824.1:n.474+302G>A
NM_000582.2:c.498+302G>A	NP_000573.1:n.498+302G>A
NM_001040058.1:c.540+302G>A	NP_001035147.1:n.540+302G>A
NM_001040060.1:c.459+302G>A	NP_001035149.1:n.459+302G>A
NM_001251829.1:c.417+302G>A	NP_001238758.1:n.417+302G>A
NM_001251830.1:c.579+302G>A	NP_001238759.1:n.579+302G>A
NM_001040058.2:c.540+302G>A MANE Select	NP_001035147.1:n.540+302G>A
NM_000582.3:c.498+302G>A	NP_000573.1:n.498+302G>A
NM_001040060.2:c.459+302G>A	NP_001035149.1:n.459+302G>A
NM_001251829.2:c.417+302G>A	NP_001238758.1:n.417+302G>A
NM_001251830.2:c.579+302G>A	NP_001238759.1:n.579+302G>A