Canonical Allele Identifier: CA1590779768
Gene: CSF1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150073489_150073491delinsACT , CM000667.2:g.150073489_150073491delinsACT GRCh38
NC_000005.9:g.149453052_149453054delinsACT , CM000667.1:g.149453052_149453054delinsACT GRCh37
NC_000005.8:g.149433245_149433247delinsACT NCBI36
NG_012303.1:g.44882_44884delinsAGT
NG_012303.2:g.44882_44884delinsAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000675795.1:c.892_894delinsAGT MANE Select ENSP00000501699.1:p.Ser298=
ENST00000286301.7:c.892_894delinsAGT ENSP00000286301.3:p.Ser298=
ENST00000504875.5:c.892_894delinsAGT ENSP00000422212.1:p.Ser298=
ENST00000543093.1:c.890-2920_890-2918delinsAGT ENSP00000445282.1:n.890-2920_890-2918delinsAGT
NM_001288705.1:c.892_894delinsAGT NP_001275634.1:p.Ser298=
NM_005211.3:c.892_894delinsAGT NP_005202.2:p.Ser298=
NR_109969.1:n.1105_1107delinsAGT
NM_001288705.2:c.892_894delinsAGT NP_001275634.1:p.Ser298=
NM_001349736.1:c.892_894delinsAGT NP_001336665.1:p.Ser298=
NM_001288705.3:c.892_894delinsAGT MANE Select NP_001275634.1:p.Ser298=
NM_001375320.1:c.892_894delinsAGT NP_001362249.1:p.Ser298=
NM_001375321.1:c.448_450delinsAGT NP_001362250.1:p.Ser150=
NR_164679.1:n.948_950delinsAGT
NM_001349736.2:c.892_894delinsAGT NP_001336665.1:p.Ser298=
NM_005211.4:c.892_894delinsAGT NP_005202.2:p.Ser298=
NR_109969.2:n.1019_1021delinsAGT