Canonical Allele Identifier: CA3003613

Gene: SPP1

Linked Data

• dbSNP Id: rs374055797
• ExAC: 4:88903635 G / A
• gnomAD v2: 4-88903635-G-A
• gnomAD v3: 4-87982483-G-A
• gnomAD v4: 4-87982483-G-A
• MyVariant Identifiers: chr4:g.88903635G>A (hg19) ; chr4:g.87982483G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982483G>A , CM000666.2:g.87982483G>A	GRCh38
NC_000004.11:g.88903635G>A , CM000666.1:g.88903635G>A	GRCh37
NC_000004.10:g.89122659G>A	NCBI36
NG_030362.1:g.11834G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.418-9G>A	ENSP00000422973.2:n.418-9G>A
ENST00000614857.5:c.541-9G>A	ENSP00000477824.2:n.541-9G>A
ENST00000681973.1:n.768-9G>A
ENST00000682026.1:n.494-9G>A
ENST00000682448.1:n.2027-9G>A
ENST00000682554.1:n.1989-9G>A
ENST00000682599.1:n.3029-9G>A
ENST00000682627.1:n.461-9G>A
ENST00000682865.1:n.825-9G>A
ENST00000683087.1:n.555-9G>A
ENST00000683168.1:n.1295-9G>A
ENST00000683620.1:n.1723-9G>A
ENST00000684106.1:n.2791-9G>A
ENST00000684450.1:n.1600-9G>A
ENST00000684710.1:n.1832-9G>A
ENST00000395080.8:c.541-9G>A MANE Select	ENSP00000378517.3:n.541-9G>A
ENST00000237623.11:c.499-9G>A	ENSP00000237623.7:n.499-9G>A
ENST00000360804.4:c.460-9G>A	ENSP00000354042.4:n.460-9G>A
ENST00000395080.7:c.541-9G>A	ENSP00000378517.3:n.541-9G>A
ENST00000508233.5:c.418-9G>A	ENSP00000422973.1:n.418-9G>A
ENST00000509659.5:n.830-9G>A
ENST00000614857.4:c.475-9G>A	ENSP00000477824.1:n.475-9G>A
NM_000582.2:c.499-9G>A	NP_000573.1:n.499-9G>A
NM_001040058.1:c.541-9G>A	NP_001035147.1:n.541-9G>A
NM_001040060.1:c.460-9G>A	NP_001035149.1:n.460-9G>A
NM_001251829.1:c.418-9G>A	NP_001238758.1:n.418-9G>A
NM_001251830.1:c.580-9G>A	NP_001238759.1:n.580-9G>A
NM_001040058.2:c.541-9G>A MANE Select	NP_001035147.1:n.541-9G>A
NM_000582.3:c.499-9G>A	NP_000573.1:n.499-9G>A
NM_001040060.2:c.460-9G>A	NP_001035149.1:n.460-9G>A
NM_001251829.2:c.418-9G>A	NP_001238758.1:n.418-9G>A
NM_001251830.2:c.580-9G>A	NP_001238759.1:n.580-9G>A