Canonical Allele Identifier: CA3506363

Gene: CSF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150054323C>G , CM000667.2:g.150054323C>G	GRCh38
NC_000005.9:g.149433886C>G , CM000667.1:g.149433886C>G	GRCh37
NC_000005.8:g.149414079C>G	NCBI36
NG_012303.1:g.64050G>C
NG_021389.1:g.58718C>G
NG_012303.2:g.64050G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001288705.3:c.2762G>C MANE Select	NP_001275634.1:p.Arg921Pro
ENST00000675795.1:c.2762G>C MANE Select	ENSP00000501699.1:p.Arg921Pro
NM_001288705.1:c.2762G>C	NP_001275634.1:p.Arg921Pro
NM_001288705.2:c.2762G>C	NP_001275634.1:p.Arg921Pro
NM_001349736.1:c.2762G>C	NP_001336665.1:p.Arg921Pro
NM_001349736.2:c.2762G>C	NP_001336665.1:p.Arg921Pro
NM_001375320.1:c.2762G>C	NP_001362249.1:p.Arg921Pro
NM_001375321.1:c.2318G>C	NP_001362250.1:p.Arg773Pro
NM_005211.3:c.2762G>C	NP_005202.2:p.Arg921Pro
NM_005211.4:c.2762G>C	NP_005202.2:p.Arg921Pro
NR_109969.1:n.2812G>C
NR_109969.2:n.2726G>C
NR_164679.1:n.2655G>C
ENST00000286301.7:c.2762G>C	ENSP00000286301.3:p.Arg921Pro
ENST00000504875.5:c.*583G>C	ENSP00000422212.1:n.*583G>C
ENST00000509861.1:n.498G>C