Canonical Allele Identifier: CA1590779894
Gene: CSF1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150073804T= , CM000667.2:g.150073804T= GRCh38
NC_000005.9:g.149453367T= , CM000667.1:g.149453367T= GRCh37
NC_000005.8:g.149433560T= NCBI36
NG_012303.1:g.44569A=
NG_012303.2:g.44569A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000675795.1:c.890-311A= MANE Select ENSP00000501699.1:n.890-311A=
ENST00000286301.7:c.890-311A= ENSP00000286301.3:n.890-311A=
ENST00000504875.5:c.890-311A= ENSP00000422212.1:n.890-311A=
ENST00000543093.1:c.890-3233A= ENSP00000445282.1:n.890-3233A=
NM_001288705.1:c.890-311A= NP_001275634.1:n.890-311A=
NM_005211.3:c.890-311A= NP_005202.2:n.890-311A=
NR_109969.1:n.1103-311A=
NM_001288705.2:c.890-311A= NP_001275634.1:n.890-311A=
NM_001349736.1:c.890-311A= NP_001336665.1:n.890-311A=
NM_001288705.3:c.890-311A= MANE Select NP_001275634.1:n.890-311A=
NM_001375320.1:c.890-311A= NP_001362249.1:n.890-311A=
NM_001375321.1:c.446-311A= NP_001362250.1:n.446-311A=
NR_164679.1:n.946-311A=
NM_001349736.2:c.890-311A= NP_001336665.1:n.890-311A=
NM_005211.4:c.890-311A= NP_005202.2:n.890-311A=
NR_109969.2:n.1017-311A=