Canonical Allele Identifier: CA2671367286

Gene: SPP1

Linked Data

• gnomAD v4: 4-87981917-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87981917T>C , CM000666.2:g.87981917T>C	GRCh38
NC_000004.11:g.88903069T>C , CM000666.1:g.88903069T>C	GRCh37
NC_000004.10:g.89122093T>C	NCBI36
NG_030362.1:g.11268T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508233.6:c.417+119T>C	ENSP00000422973.2:n.417+119T>C
ENST00000614857.5:c.540+119T>C	ENSP00000477824.2:n.540+119T>C
ENST00000681973.1:n.767+119T>C
ENST00000682026.1:n.493+119T>C
ENST00000682448.1:n.2026+119T>C
ENST00000682554.1:n.1988+119T>C
ENST00000682599.1:n.3028+119T>C
ENST00000682627.1:n.460+119T>C
ENST00000682655.1:c.*80T>C	ENSP00000508280.1:n.*80T>C
ENST00000682865.1:n.824+119T>C
ENST00000683087.1:n.554+119T>C
ENST00000683168.1:n.1294+119T>C
ENST00000683620.1:n.1722+119T>C
ENST00000684106.1:n.2790+119T>C
ENST00000684450.1:n.1599+119T>C
ENST00000684710.1:n.1831+119T>C
ENST00000395080.8:c.540+119T>C MANE Select	ENSP00000378517.3:n.540+119T>C
ENST00000237623.11:c.498+119T>C	ENSP00000237623.7:n.498+119T>C
ENST00000360804.4:c.459+119T>C	ENSP00000354042.4:n.459+119T>C
ENST00000395080.7:c.540+119T>C	ENSP00000378517.3:n.540+119T>C
ENST00000508233.5:c.417+119T>C	ENSP00000422973.1:n.417+119T>C
ENST00000509659.5:n.829+119T>C
ENST00000614857.4:c.474+119T>C	ENSP00000477824.1:n.474+119T>C
NM_000582.2:c.498+119T>C	NP_000573.1:n.498+119T>C
NM_001040058.1:c.540+119T>C	NP_001035147.1:n.540+119T>C
NM_001040060.1:c.459+119T>C	NP_001035149.1:n.459+119T>C
NM_001251829.1:c.417+119T>C	NP_001238758.1:n.417+119T>C
NM_001251830.1:c.579+119T>C	NP_001238759.1:n.579+119T>C
NM_001040058.2:c.540+119T>C MANE Select	NP_001035147.1:n.540+119T>C
NM_000582.3:c.498+119T>C	NP_000573.1:n.498+119T>C
NM_001040060.2:c.459+119T>C	NP_001035149.1:n.459+119T>C
NM_001251829.2:c.417+119T>C	NP_001238758.1:n.417+119T>C
NM_001251830.2:c.579+119T>C	NP_001238759.1:n.579+119T>C