Canonical Allele Identifier: CA1590772954

Gene: CSF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150057345T= , CM000667.2:g.150057345T=	GRCh38
NC_000005.9:g.149436908T= , CM000667.1:g.149436908T=	GRCh37
NC_000005.8:g.149417101T=	NCBI36
NG_012303.1:g.61028A=
NG_012303.2:g.61028A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675795.1:c.2261A= MANE Select	ENSP00000501699.1:p.Asp754=
ENST00000286301.7:c.2261A=	ENSP00000286301.3:p.Asp754=
ENST00000504875.5:c.*82A=	ENSP00000422212.1:n.*82A=
ENST00000515068.1:c.430A=	ENSP00000427545.1:n.430A=
NM_001288705.1:c.2261A=	NP_001275634.1:p.Asp754=
NM_005211.3:c.2261A=	NP_005202.2:p.Asp754=
NR_109969.1:n.2311A=
NM_001288705.2:c.2261A=	NP_001275634.1:p.Asp754=
NM_001349736.1:c.2261A=	NP_001336665.1:p.Asp754=
NM_001288705.3:c.2261A= MANE Select	NP_001275634.1:p.Asp754=
NM_001375320.1:c.2261A=	NP_001362249.1:p.Asp754=
NM_001375321.1:c.1817A=	NP_001362250.1:p.Asp606=
NR_164679.1:n.2154A=
NM_001349736.2:c.2261A=	NP_001336665.1:p.Asp754=
NM_005211.4:c.2261A=	NP_005202.2:p.Asp754=
NR_109969.2:n.2225A=