Canonical Allele Identifier: CA361758295
Community Standard Title: NM_001288705.3(CSF1R):c.2541G>T (p.Glu847Asp)
Gene: CSF1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150056039C>A , CM000667.2:g.150056039C>A GRCh38
NC_000005.9:g.149435602C>A , CM000667.1:g.149435602C>A GRCh37
NC_000005.8:g.149415795C>A NCBI36
NG_012303.1:g.62334G>T
NG_012303.2:g.62334G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001288705.3:c.2541G>T MANE Select NP_001275634.1:p.Glu847Asp
ENST00000675795.1:c.2541G>T MANE Select ENSP00000501699.1:p.Glu847Asp
NM_001288705.1:c.2541G>T NP_001275634.1:p.Glu847Asp
NM_001288705.2:c.2541G>T NP_001275634.1:p.Glu847Asp
NM_001349736.1:c.2541G>T NP_001336665.1:p.Glu847Asp
NM_001349736.2:c.2541G>T NP_001336665.1:p.Glu847Asp
NM_001375320.1:c.2541G>T NP_001362249.1:p.Glu847Asp
NM_001375321.1:c.2097G>T NP_001362250.1:p.Glu699Asp
NM_005211.3:c.2541G>T NP_005202.2:p.Glu847Asp
NM_005211.4:c.2541G>T NP_005202.2:p.Glu847Asp
NR_109969.1:n.2591G>T
NR_109969.2:n.2505G>T
NR_164679.1:n.2434G>T
ENST00000286301.7:c.2541G>T ENSP00000286301.3:p.Glu847Asp
ENST00000504875.5:c.*362G>T ENSP00000422212.1:n.*362G>T
ENST00000515068.1:c.710G>T ENSP00000427545.1:n.710G>T