Canonical Allele Identifier: CA1590773000

Gene: CSF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150057425C= , CM000667.2:g.150057425C=	GRCh38
NC_000005.9:g.149436988C= , CM000667.1:g.149436988C=	GRCh37
NC_000005.8:g.149417181C=	NCBI36
NG_012303.1:g.60948G=
NG_012303.2:g.60948G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675795.1:c.2222-41G= MANE Select	ENSP00000501699.1:n.2222-41G=
ENST00000286301.7:c.2222-41G=	ENSP00000286301.3:n.2222-41G=
ENST00000504875.5:c.*43-41G=	ENSP00000422212.1:n.*43-41G=
ENST00000515068.1:c.391-41G=	ENSP00000427545.1:n.391-41G=
NM_001288705.1:c.2222-41G=	NP_001275634.1:n.2222-41G=
NM_005211.3:c.2222-41G=	NP_005202.2:n.2222-41G=
NR_109969.1:n.2272-41G=
NM_001288705.2:c.2222-41G=	NP_001275634.1:n.2222-41G=
NM_001349736.1:c.2222-41G=	NP_001336665.1:n.2222-41G=
NM_001288705.3:c.2222-41G= MANE Select	NP_001275634.1:n.2222-41G=
NM_001375320.1:c.2222-41G=	NP_001362249.1:n.2222-41G=
NM_001375321.1:c.1778-41G=	NP_001362250.1:n.1778-41G=
NR_164679.1:n.2115-41G=
NM_001349736.2:c.2222-41G=	NP_001336665.1:n.2222-41G=
NM_005211.4:c.2222-41G=	NP_005202.2:n.2222-41G=
NR_109969.2:n.2186-41G=