Canonical Allele Identifier: CA361760030
Gene: CSF1R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150057318G>T , CM000667.2:g.150057318G>T GRCh38
NC_000005.9:g.149436881G>T , CM000667.1:g.149436881G>T GRCh37
NC_000005.8:g.149417074G>T NCBI36
NG_012303.1:g.61055C>A
NG_012303.2:g.61055C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000675795.1:c.2288C>A MANE Select ENSP00000501699.1:p.Ala763Asp
ENST00000286301.7:c.2288C>A ENSP00000286301.3:p.Ala763Asp
ENST00000504875.5:c.*109C>A ENSP00000422212.1:n.*109C>A
ENST00000515068.1:c.457C>A ENSP00000427545.1:n.457C>A
NM_001288705.1:c.2288C>A NP_001275634.1:p.Ala763Asp
NM_005211.3:c.2288C>A NP_005202.2:p.Ala763Asp
NR_109969.1:n.2338C>A
NM_001288705.2:c.2288C>A NP_001275634.1:p.Ala763Asp
NM_001349736.1:c.2288C>A NP_001336665.1:p.Ala763Asp
NM_001288705.3:c.2288C>A MANE Select NP_001275634.1:p.Ala763Asp
NM_001375320.1:c.2288C>A NP_001362249.1:p.Ala763Asp
NM_001375321.1:c.1844C>A NP_001362250.1:p.Ala615Asp
NR_164679.1:n.2181C>A
NM_001349736.2:c.2288C>A NP_001336665.1:p.Ala763Asp
NM_005211.4:c.2288C>A NP_005202.2:p.Ala763Asp
NR_109969.2:n.2252C>A