Canonical Allele Identifier: CA048710
Gene: CSF3R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.36472276_36472291del , CM000663.2:g.36472276_36472291del GRCh38
NC_000001.10:g.36937877_36937892del , CM000663.1:g.36937877_36937892del GRCh37
NC_000001.9:g.36710464_36710479del NCBI36
NG_016270.1:g.15622_15637del , LRG_144:g.15622_15637del

Transcript Alleles

HGVS Amino-acid Change
ENST00000464465.7:c.948_963del ENSP00000435218.2:p.His317AlafsTer6
ENST00000487540.7:c.948_963del ENSP00000514169.2:p.His317AlafsTer6
ENST00000464365.3:n.1806_1821del
ENST00000699089.1:n.1928_1943del
ENST00000699090.1:c.552_567del ENSP00000514168.1:p.His185AlafsTer6
ENST00000373106.6:c.948_963del MANE Select ENSP00000362198.2:p.His317AlafsTer6
ENST00000331941.6:c.948_963del ENSP00000332180.5:p.His317AlafsTer6
ENST00000361632.8:c.948_963del ENSP00000355406.4:p.His317AlafsTer6
ENST00000373103.5:c.948_963del ENSP00000362195.1:p.His317AlafsTer6
ENST00000373104.5:c.948_963del ENSP00000362196.1:p.His317AlafsTer6
ENST00000373106.5:c.948_963del ENSP00000362198.1:p.His317AlafsTer6
ENST00000464365.2:n.623_638del
ENST00000480825.6:n.2331_2346del
ENST00000487540.6:n.101_116del
NM_000760.3:c.948_963del NP_000751.1:p.His317AlafsTer6
NM_156039.3:c.948_963del , LRG_144t1:c.948_963del NP_724781.1:p.His317AlafsTer6
NM_172313.2:c.948_963del NP_758519.1:p.His317AlafsTer6
XM_005270493.1:c.948_963del XP_005270550.1:p.His317AlafsTer6
XM_011540748.1:c.948_963del XP_011539050.1:p.His317AlafsTer6
XM_011540749.1:c.948_963del XP_011539051.1:p.His317AlafsTer6
XM_011540750.1:c.276_291del XP_011539052.1:p.His93AlafsTer6
XM_011540748.3:c.948_963del XP_011539050.1:p.His317AlafsTer6
XM_017000370.1:c.948_963del XP_016855859.1:p.His317AlafsTer6
NM_000760.4:c.948_963del MANE Select NP_000751.1:p.His317AlafsTer6
NM_172313.3:c.948_963del NP_758519.1:p.His317AlafsTer6