Canonical Allele Identifier: CA346081

Gene: CSF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150054432T>C , CM000667.2:g.150054432T>C	GRCh38
NC_000005.9:g.149433995T>C , CM000667.1:g.149433995T>C	GRCh37
NC_000005.8:g.149414188T>C	NCBI36
NG_012303.1:g.63941A>G
NG_021389.1:g.58827T>C
NG_012303.2:g.63941A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001288705.3:c.2655-2A>G MANE Select	NP_001275634.1:n.2655-2A>G
ENST00000675795.1:c.2655-2A>G MANE Select	ENSP00000501699.1:n.2655-2A>G
NM_001288705.1:c.2655-2A>G	NP_001275634.1:n.2655-2A>G
NM_001288705.2:c.2655-2A>G	NP_001275634.1:n.2655-2A>G
NM_001349736.1:c.2655-2A>G	NP_001336665.1:n.2655-2A>G
NM_001349736.2:c.2655-2A>G	NP_001336665.1:n.2655-2A>G
NM_001375320.1:c.2655-2A>G	NP_001362249.1:n.2655-2A>G
NM_001375321.1:c.2211-2A>G	NP_001362250.1:n.2211-2A>G
NM_005211.3:c.2655-2A>G	NP_005202.2:n.2655-2A>G
NM_005211.4:c.2655-2A>G	NP_005202.2:n.2655-2A>G
NR_109969.1:n.2705-2A>G
NR_109969.2:n.2619-2A>G
NR_164679.1:n.2548-2A>G
ENST00000286301.7:c.2655-2A>G	ENSP00000286301.3:n.2655-2A>G
ENST00000504875.5:c.*476-2A>G	ENSP00000422212.1:n.*476-2A>G
ENST00000509861.1:n.389A>G