Canonical Allele Identifier: CA357618244
Gene: SPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87982513G>T , CM000666.2:g.87982513G>T GRCh38
NC_000004.11:g.88903665G>T , CM000666.1:g.88903665G>T GRCh37
NC_000004.10:g.89122689G>T NCBI36
NG_030362.1:g.11864G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000508233.6:c.439G>T ENSP00000422973.2:p.Asp147Tyr
ENST00000614857.5:c.562G>T ENSP00000477824.2:p.Asp188Tyr
ENST00000681973.1:n.789G>T
ENST00000682026.1:n.515G>T
ENST00000682448.1:n.2048G>T
ENST00000682554.1:n.2010G>T
ENST00000682599.1:n.3050G>T
ENST00000682627.1:n.482G>T
ENST00000682865.1:n.846G>T
ENST00000683087.1:n.576G>T
ENST00000683168.1:n.1316G>T
ENST00000683620.1:n.1744G>T
ENST00000684106.1:n.2812G>T
ENST00000684450.1:n.1621G>T
ENST00000684710.1:n.1853G>T
ENST00000395080.8:c.562G>T MANE Select ENSP00000378517.3:p.Asp188Tyr
ENST00000237623.11:c.520G>T ENSP00000237623.7:p.Asp174Tyr
ENST00000360804.4:c.481G>T ENSP00000354042.4:p.Asp161Tyr
ENST00000395080.7:c.562G>T ENSP00000378517.3:p.Asp188Tyr
ENST00000508233.5:c.439G>T ENSP00000422973.1:p.Asp147Tyr
ENST00000509659.5:n.851G>T
ENST00000614857.4:c.496G>T ENSP00000477824.1:p.Asp166Tyr
NM_000582.2:c.520G>T NP_000573.1:p.Asp174Tyr
NM_001040058.1:c.562G>T NP_001035147.1:p.Asp188Tyr
NM_001040060.1:c.481G>T NP_001035149.1:p.Asp161Tyr
NM_001251829.1:c.439G>T NP_001238758.1:p.Asp147Tyr
NM_001251830.1:c.601G>T NP_001238759.1:p.Asp201Tyr
NM_001040058.2:c.562G>T MANE Select NP_001035147.1:p.Asp188Tyr
NM_000582.3:c.520G>T NP_000573.1:p.Asp174Tyr
NM_001040060.2:c.481G>T NP_001035149.1:p.Asp161Tyr
NM_001251829.2:c.439G>T NP_001238758.1:p.Asp147Tyr
NM_001251830.2:c.601G>T NP_001238759.1:p.Asp201Tyr