Canonical Allele Identifier: CA2671367334
Gene: SPP1 HGNC NCBI

Linked Data

gnomAD v4: 4-87982404-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87982404G>T , CM000666.2:g.87982404G>T GRCh38
NC_000004.11:g.88903556G>T , CM000666.1:g.88903556G>T GRCh37
NC_000004.10:g.89122580G>T NCBI36
NG_030362.1:g.11755G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000508233.6:c.418-88G>T ENSP00000422973.2:n.418-88G>T
ENST00000614857.5:c.541-88G>T ENSP00000477824.2:n.541-88G>T
ENST00000681973.1:n.768-88G>T
ENST00000682026.1:n.494-88G>T
ENST00000682448.1:n.2027-88G>T
ENST00000682554.1:n.1989-88G>T
ENST00000682599.1:n.3029-88G>T
ENST00000682627.1:n.461-88G>T
ENST00000682865.1:n.825-88G>T
ENST00000683087.1:n.555-88G>T
ENST00000683168.1:n.1295-88G>T
ENST00000683620.1:n.1723-88G>T
ENST00000684106.1:n.2791-88G>T
ENST00000684450.1:n.1600-88G>T
ENST00000684710.1:n.1832-88G>T
ENST00000395080.8:c.541-88G>T MANE Select ENSP00000378517.3:n.541-88G>T
ENST00000237623.11:c.499-88G>T ENSP00000237623.7:n.499-88G>T
ENST00000360804.4:c.460-88G>T ENSP00000354042.4:n.460-88G>T
ENST00000395080.7:c.541-88G>T ENSP00000378517.3:n.541-88G>T
ENST00000508233.5:c.418-88G>T ENSP00000422973.1:n.418-88G>T
ENST00000509659.5:n.830-88G>T
ENST00000614857.4:c.475-88G>T ENSP00000477824.1:n.475-88G>T
NM_000582.2:c.499-88G>T NP_000573.1:n.499-88G>T
NM_001040058.1:c.541-88G>T NP_001035147.1:n.541-88G>T
NM_001040060.1:c.460-88G>T NP_001035149.1:n.460-88G>T
NM_001251829.1:c.418-88G>T NP_001238758.1:n.418-88G>T
NM_001251830.1:c.580-88G>T NP_001238759.1:n.580-88G>T
NM_001040058.2:c.541-88G>T MANE Select NP_001035147.1:n.541-88G>T
NM_000582.3:c.499-88G>T NP_000573.1:n.499-88G>T
NM_001040060.2:c.460-88G>T NP_001035149.1:n.460-88G>T
NM_001251829.2:c.418-88G>T NP_001238758.1:n.418-88G>T
NM_001251830.2:c.580-88G>T NP_001238759.1:n.580-88G>T