Canonical Allele Identifier: CA1590779888
Gene: CSF1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150073797G= , CM000667.2:g.150073797G= GRCh38
NC_000005.9:g.149453360G= , CM000667.1:g.149453360G= GRCh37
NC_000005.8:g.149433553G= NCBI36
NG_012303.1:g.44576C=
NG_012303.2:g.44576C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000675795.1:c.890-304C= MANE Select ENSP00000501699.1:n.890-304C=
ENST00000286301.7:c.890-304C= ENSP00000286301.3:n.890-304C=
ENST00000504875.5:c.890-304C= ENSP00000422212.1:n.890-304C=
ENST00000543093.1:c.890-3226C= ENSP00000445282.1:n.890-3226C=
NM_001288705.1:c.890-304C= NP_001275634.1:n.890-304C=
NM_005211.3:c.890-304C= NP_005202.2:n.890-304C=
NR_109969.1:n.1103-304C=
NM_001288705.2:c.890-304C= NP_001275634.1:n.890-304C=
NM_001349736.1:c.890-304C= NP_001336665.1:n.890-304C=
NM_001288705.3:c.890-304C= MANE Select NP_001275634.1:n.890-304C=
NM_001375320.1:c.890-304C= NP_001362249.1:n.890-304C=
NM_001375321.1:c.446-304C= NP_001362250.1:n.446-304C=
NR_164679.1:n.946-304C=
NM_001349736.2:c.890-304C= NP_001336665.1:n.890-304C=
NM_005211.4:c.890-304C= NP_005202.2:n.890-304C=
NR_109969.2:n.1017-304C=