Canonical Allele Identifier: CA1590779764
Gene: CSF1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150073483G= , CM000667.2:g.150073483G= GRCh38
NC_000005.9:g.149453046G= , CM000667.1:g.149453046G= GRCh37
NC_000005.8:g.149433239G= NCBI36
NG_012303.1:g.44890C=
NG_012303.2:g.44890C=

Transcript Alleles

HGVS Amino-acid change
ENST00000675795.1:c.900C= MANE Select ENSP00000501699.1:p.Tyr300=
ENST00000286301.7:c.900C= ENSP00000286301.3:p.Tyr300=
ENST00000504875.5:c.900C= ENSP00000422212.1:p.Tyr300=
ENST00000543093.1:c.890-2912C= ENSP00000445282.1:n.890-2912C=
NM_001288705.1:c.900C= NP_001275634.1:p.Tyr300=
NM_005211.3:c.900C= NP_005202.2:p.Tyr300=
NR_109969.1:n.1113C=
NM_001288705.2:c.900C= NP_001275634.1:p.Tyr300=
NM_001349736.1:c.900C= NP_001336665.1:p.Tyr300=
NM_001288705.3:c.900C= MANE Select NP_001275634.1:p.Tyr300=
NM_001375320.1:c.900C= NP_001362249.1:p.Tyr300=
NM_001375321.1:c.456C= NP_001362250.1:p.Tyr152=
NR_164679.1:n.956C=
NM_001349736.2:c.900C= NP_001336665.1:p.Tyr300=
NM_005211.4:c.900C= NP_005202.2:p.Tyr300=
NR_109969.2:n.1027C=