Canonical Allele Identifier: CA2671367359
Gene: SPP1 HGNC NCBI

Linked Data

gnomAD v4: 4-87982488-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87982488T>A , CM000666.2:g.87982488T>A GRCh38
NC_000004.11:g.88903640T>A , CM000666.1:g.88903640T>A GRCh37
NC_000004.10:g.89122664T>A NCBI36
NG_030362.1:g.11839T>A

Transcript Alleles

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