Canonical Allele Identifier: CA769156

Gene: CSF3R

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.36469204C>G , CM000663.2:g.36469204C>G	GRCh38
NC_000001.10:g.36934805C>G , CM000663.1:g.36934805C>G	GRCh37
NC_000001.9:g.36707392C>G	NCBI36
NG_016270.1:g.18705G>C , LRG_144:g.18705G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464465.7:c.1474+448G>C	ENSP00000435218.2:n.1474+448G>C
ENST00000487540.7:c.1528G>C	ENSP00000514169.2:p.Asp510His
ENST00000464365.3:n.2386G>C
ENST00000699089.1:n.2508G>C
ENST00000699090.1:c.1132G>C	ENSP00000514168.1:p.Asp378His
ENST00000373106.6:c.1528G>C MANE Select	ENSP00000362198.2:p.Asp510His
ENST00000331941.6:c.1528G>C	ENSP00000332180.5:p.Asp510His
ENST00000361632.8:c.1528G>C	ENSP00000355406.4:p.Asp510His
ENST00000373103.5:c.1528G>C	ENSP00000362195.1:p.Asp510His
ENST00000373104.5:c.1528G>C	ENSP00000362196.1:p.Asp510His
ENST00000373106.5:c.1528G>C	ENSP00000362198.1:p.Asp510His
ENST00000464365.2:n.1203G>C
ENST00000464465.6:c.231+448G>C
ENST00000480825.6:n.3330G>C
ENST00000487540.6:n.681G>C
NM_000760.3:c.1528G>C	NP_000751.1:p.Asp510His
NM_156039.3:c.1528G>C , LRG_144t1:c.1528G>C	NP_724781.1:p.Asp510His
NM_172313.2:c.1528G>C	NP_758519.1:p.Asp510His
XM_005270493.1:c.1528G>C	XP_005270550.1:p.Asp510His
XM_011540748.1:c.1528G>C	XP_011539050.1:p.Asp510His
XM_011540749.1:c.1528G>C	XP_011539051.1:p.Asp510His
XM_011540750.1:c.856G>C	XP_011539052.1:p.Asp286His
XM_011540748.3:c.1528G>C	XP_011539050.1:p.Asp510His
XM_017000370.1:c.1528G>C	XP_016855859.1:p.Asp510His
NM_000760.4:c.1528G>C MANE Select	NP_000751.1:p.Asp510His
NM_172313.3:c.1528G>C	NP_758519.1:p.Asp510His