Canonical Allele Identifier: CA361714182

Gene: CSF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150061584C>T , CM000667.2:g.150061584C>T	GRCh38
NC_000005.9:g.149441147C>T , CM000667.1:g.149441147C>T	GRCh37
NC_000005.8:g.149421340C>T	NCBI36
NG_012303.1:g.56789G>A
NG_012303.2:g.56789G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001288705.3:c.1765G>A MANE Select	NP_001275634.1:p.Gly589Arg
ENST00000675795.1:c.1765G>A MANE Select	ENSP00000501699.1:p.Gly589Arg
NM_001288705.1:c.1765G>A	NP_001275634.1:p.Gly589Arg
NM_001288705.2:c.1765G>A	NP_001275634.1:p.Gly589Arg
NM_001349736.1:c.1765G>A	NP_001336665.1:p.Gly589Arg
NM_001349736.2:c.1765G>A	NP_001336665.1:p.Gly589Arg
NM_001375320.1:c.1765G>A	NP_001362249.1:p.Gly589Arg
NM_001375321.1:c.1321G>A	NP_001362250.1:p.Gly441Arg
NM_005211.3:c.1765G>A	NP_005202.2:p.Gly589Arg
NM_005211.4:c.1765G>A	NP_005202.2:p.Gly589Arg
NR_109969.1:n.1978G>A
NR_109969.2:n.1892G>A
NR_164679.1:n.1821G>A
ENST00000286301.7:c.1765G>A	ENSP00000286301.3:p.Gly589Arg
ENST00000504875.5:c.1765G>A	ENSP00000422212.1:p.Gly589Arg
ENST00000513609.1:n.422G>A
ENST00000515068.1:c.73+12G>A	ENSP00000427545.1:n.73+12G>A
ENST00000515239.5:n.295G>A