Canonical Allele Identifier: CA357618179
Gene: SPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87982498G>A , CM000666.2:g.87982498G>A GRCh38
NC_000004.11:g.88903650G>A , CM000666.1:g.88903650G>A GRCh37
NC_000004.10:g.89122674G>A NCBI36
NG_030362.1:g.11849G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000508233.6:c.424G>A ENSP00000422973.2:p.Asp142Asn
ENST00000614857.5:c.547G>A ENSP00000477824.2:p.Asp183Asn
ENST00000681973.1:n.774G>A
ENST00000682026.1:n.500G>A
ENST00000682448.1:n.2033G>A
ENST00000682554.1:n.1995G>A
ENST00000682599.1:n.3035G>A
ENST00000682627.1:n.467G>A
ENST00000682865.1:n.831G>A
ENST00000683087.1:n.561G>A
ENST00000683168.1:n.1301G>A
ENST00000683620.1:n.1729G>A
ENST00000684106.1:n.2797G>A
ENST00000684450.1:n.1606G>A
ENST00000684710.1:n.1838G>A
ENST00000395080.8:c.547G>A MANE Select ENSP00000378517.3:p.Asp183Asn
ENST00000237623.11:c.505G>A ENSP00000237623.7:p.Asp169Asn
ENST00000360804.4:c.466G>A ENSP00000354042.4:p.Asp156Asn
ENST00000395080.7:c.547G>A ENSP00000378517.3:p.Asp183Asn
ENST00000508233.5:c.424G>A ENSP00000422973.1:p.Asp142Asn
ENST00000509659.5:n.836G>A
ENST00000614857.4:c.481G>A ENSP00000477824.1:p.Asp161Asn
NM_000582.2:c.505G>A NP_000573.1:p.Asp169Asn
NM_001040058.1:c.547G>A NP_001035147.1:p.Asp183Asn
NM_001040060.1:c.466G>A NP_001035149.1:p.Asp156Asn
NM_001251829.1:c.424G>A NP_001238758.1:p.Asp142Asn
NM_001251830.1:c.586G>A NP_001238759.1:p.Asp196Asn
NM_001040058.2:c.547G>A MANE Select NP_001035147.1:p.Asp183Asn
NM_000582.3:c.505G>A NP_000573.1:p.Asp169Asn
NM_001040060.2:c.466G>A NP_001035149.1:p.Asp156Asn
NM_001251829.2:c.424G>A NP_001238758.1:p.Asp142Asn
NM_001251830.2:c.586G>A NP_001238759.1:p.Asp196Asn