Canonical Allele Identifier: CA1590779690

Gene: CSF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150073291T= , CM000667.2:g.150073291T=	GRCh38
NC_000005.9:g.149452854T= , CM000667.1:g.149452854T=	GRCh37
NC_000005.8:g.149433047T=	NCBI36
NG_012303.1:g.45082A=
NG_012303.2:g.45082A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675795.1:c.1082+10A= MANE Select	ENSP00000501699.1:n.1082+10A=
ENST00000286301.7:c.1082+10A=	ENSP00000286301.3:n.1082+10A=
ENST00000504875.5:c.1082+10A=	ENSP00000422212.1:n.1082+10A=
ENST00000543093.1:c.890-2720A=	ENSP00000445282.1:n.890-2720A=
NM_001288705.1:c.1082+10A=	NP_001275634.1:n.1082+10A=
NM_005211.3:c.1082+10A=	NP_005202.2:n.1082+10A=
NR_109969.1:n.1295+10A=
NM_001288705.2:c.1082+10A=	NP_001275634.1:n.1082+10A=
NM_001349736.1:c.1082+10A=	NP_001336665.1:n.1082+10A=
NM_001288705.3:c.1082+10A= MANE Select	NP_001275634.1:n.1082+10A=
NM_001375320.1:c.1082+10A=	NP_001362249.1:n.1082+10A=
NM_001375321.1:c.638+10A=	NP_001362250.1:n.638+10A=
NR_164679.1:n.1138+10A=
NM_001349736.2:c.1082+10A=	NP_001336665.1:n.1082+10A=
NM_005211.4:c.1082+10A=	NP_005202.2:n.1082+10A=
NR_109969.2:n.1209+10A=