Canonical Allele Identifier: CA100858120

Gene: SPP1

Linked Data

• dbSNP Id: rs764812056
• gnomAD v2: 4-88903423-T-C
• gnomAD v3: 4-87982271-T-C
• gnomAD v4: 4-87982271-T-C
• MyVariant Identifiers: chr4:g.88903423T>C (hg19) ; chr4:g.87982271T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87982271T>C , CM000666.2:g.87982271T>C	GRCh38
NC_000004.11:g.88903423T>C , CM000666.1:g.88903423T>C	GRCh37
NC_000004.10:g.89122447T>C	NCBI36
NG_030362.1:g.11622T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.418-221T>C	ENSP00000422973.2:n.418-221T>C
ENST00000614857.5:c.541-221T>C	ENSP00000477824.2:n.541-221T>C
ENST00000681973.1:n.768-221T>C
ENST00000682026.1:n.494-221T>C
ENST00000682448.1:n.2027-221T>C
ENST00000682554.1:n.1989-221T>C
ENST00000682599.1:n.3029-221T>C
ENST00000682627.1:n.461-221T>C
ENST00000682865.1:n.825-221T>C
ENST00000683087.1:n.555-221T>C
ENST00000683168.1:n.1295-221T>C
ENST00000683620.1:n.1723-221T>C
ENST00000684106.1:n.2791-221T>C
ENST00000684450.1:n.1600-221T>C
ENST00000684710.1:n.1832-221T>C
ENST00000395080.8:c.541-221T>C MANE Select	ENSP00000378517.3:n.541-221T>C
ENST00000237623.11:c.499-221T>C	ENSP00000237623.7:n.499-221T>C
ENST00000360804.4:c.460-221T>C	ENSP00000354042.4:n.460-221T>C
ENST00000395080.7:c.541-221T>C	ENSP00000378517.3:n.541-221T>C
ENST00000508233.5:c.418-221T>C	ENSP00000422973.1:n.418-221T>C
ENST00000509659.5:n.830-221T>C
ENST00000614857.4:c.475-221T>C	ENSP00000477824.1:n.475-221T>C
NM_000582.2:c.499-221T>C	NP_000573.1:n.499-221T>C
NM_001040058.1:c.541-221T>C	NP_001035147.1:n.541-221T>C
NM_001040060.1:c.460-221T>C	NP_001035149.1:n.460-221T>C
NM_001251829.1:c.418-221T>C	NP_001238758.1:n.418-221T>C
NM_001251830.1:c.580-221T>C	NP_001238759.1:n.580-221T>C
NM_001040058.2:c.541-221T>C MANE Select	NP_001035147.1:n.541-221T>C
NM_000582.3:c.499-221T>C	NP_000573.1:n.499-221T>C
NM_001040060.2:c.460-221T>C	NP_001035149.1:n.460-221T>C
NM_001251829.2:c.418-221T>C	NP_001238758.1:n.418-221T>C
NM_001251830.2:c.580-221T>C	NP_001238759.1:n.580-221T>C