Canonical Allele Identifier: CA3506401
Community Standard Title: NM_001288705.3(CSF1R):c.2603T>G (p.Leu868Arg)
Gene: CSF1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150055288A>C , CM000667.2:g.150055288A>C GRCh38
NC_000005.9:g.149434851A>C , CM000667.1:g.149434851A>C GRCh37
NC_000005.8:g.149415044A>C NCBI36
NG_012303.1:g.63085T>G
NG_012303.2:g.63085T>G

Transcript Alleles

HGVS Amino-acid Change
NM_001288705.3:c.2603T>G MANE Select NP_001275634.1:p.Leu868Arg
ENST00000675795.1:c.2603T>G MANE Select ENSP00000501699.1:p.Leu868Arg
NM_001288705.1:c.2603T>G NP_001275634.1:p.Leu868Arg
NM_001288705.2:c.2603T>G NP_001275634.1:p.Leu868Arg
NM_001349736.1:c.2603T>G NP_001336665.1:p.Leu868Arg
NM_001349736.2:c.2603T>G NP_001336665.1:p.Leu868Arg
NM_001375320.1:c.2603T>G NP_001362249.1:p.Leu868Arg
NM_001375321.1:c.2159T>G NP_001362250.1:p.Leu720Arg
NM_005211.3:c.2603T>G NP_005202.2:p.Leu868Arg
NM_005211.4:c.2603T>G NP_005202.2:p.Leu868Arg
NR_109969.1:n.2653T>G
NR_109969.2:n.2567T>G
NR_164679.1:n.2496T>G
ENST00000286301.7:c.2603T>G ENSP00000286301.3:p.Leu868Arg
ENST00000504875.5:c.*424T>G ENSP00000422212.1:n.*424T>G