Canonical Allele Identifier: CA1148224236

Gene: CSF3R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.36472313G= , CM000663.2:g.36472313G=	GRCh38
NC_000001.10:g.36937914G= , CM000663.1:g.36937914G=	GRCh37
NC_000001.9:g.36710501G=	NCBI36
NG_016270.1:g.15596C= , LRG_144:g.15596C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464465.7:c.922C=	ENSP00000435218.2:p.Arg308=
ENST00000487540.7:c.922C=	ENSP00000514169.2:p.Arg308=
ENST00000464365.3:n.1780C=
ENST00000699089.1:n.1902C=
ENST00000699090.1:c.526C=	ENSP00000514168.1:p.Arg176=
ENST00000373106.6:c.922C= MANE Select	ENSP00000362198.2:p.Arg308=
ENST00000331941.6:c.922C=	ENSP00000332180.5:p.Arg308=
ENST00000361632.8:c.922C=	ENSP00000355406.4:p.Arg308=
ENST00000373103.5:c.922C=	ENSP00000362195.1:p.Arg308=
ENST00000373104.5:c.922C=	ENSP00000362196.1:p.Arg308=
ENST00000373106.5:c.922C=	ENSP00000362198.1:p.Arg308=
ENST00000464365.2:n.597C=
ENST00000480825.6:n.2305C=
ENST00000487540.6:n.75C=
NM_000760.3:c.922C=	NP_000751.1:p.Arg308=
NM_156039.3:c.922C= , LRG_144t1:c.922C=	NP_724781.1:p.Arg308=
NM_172313.2:c.922C=	NP_758519.1:p.Arg308=
XM_005270493.1:c.922C=	XP_005270550.1:p.Arg308=
XM_011540748.1:c.922C=	XP_011539050.1:p.Arg308=
XM_011540749.1:c.922C=	XP_011539051.1:p.Arg308=
XM_011540750.1:c.250C=	XP_011539052.1:p.Arg84=
XM_011540748.3:c.922C=	XP_011539050.1:p.Arg308=
XM_017000370.1:c.922C=	XP_016855859.1:p.Arg308=
NM_000760.4:c.922C= MANE Select	NP_000751.1:p.Arg308=
NM_172313.3:c.922C=	NP_758519.1:p.Arg308=