Canonical Allele Identifier: CA339415984

Gene: CSF3R

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.36466902C>G , CM000663.2:g.36466902C>G	GRCh38
NC_000001.10:g.36932503C>G , CM000663.1:g.36932503C>G	GRCh37
NC_000001.9:g.36705090C>G	NCBI36
NG_016270.1:g.21007G>C , LRG_144:g.21007G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464465.7:c.1939-75G>C	ENSP00000435218.2:n.1939-75G>C
ENST00000487540.7:c.*335-75G>C	ENSP00000514169.2:n.*335-75G>C
ENST00000699089.1:n.3021-75G>C
ENST00000699090.1:c.1645-75G>C	ENSP00000514168.1:n.1645-75G>C
ENST00000373106.6:c.2041-75G>C MANE Select	ENSP00000362198.2:n.2041-75G>C
ENST00000331941.6:c.2041-75G>C	ENSP00000332180.5:n.2041-75G>C
ENST00000361632.8:c.2041-75G>C	ENSP00000355406.4:n.2041-75G>C
ENST00000373103.5:c.2047G>C	ENSP00000362195.1:p.Gly683Arg
ENST00000373104.5:c.2041-75G>C	ENSP00000362196.1:n.2041-75G>C
ENST00000373106.5:c.2041-75G>C	ENSP00000362198.1:n.2041-75G>C
ENST00000464465.6:c.696-75G>C
ENST00000480825.6:n.5216G>C
ENST00000484762.1:n.432-75G>C
ENST00000487540.6:n.1222-75G>C
NM_000760.3:c.2041-75G>C	NP_000751.1:n.2041-75G>C
NM_156039.3:c.2047G>C , LRG_144t1:c.2047G>C	NP_724781.1:p.Gly683Arg
NM_172313.2:c.2041-75G>C	NP_758519.1:n.2041-75G>C
XM_005270493.1:c.2038-75G>C	XP_005270550.1:n.2038-75G>C
XM_011540748.1:c.2047G>C	XP_011539050.1:p.Gly683Arg
XM_011540749.1:c.2044G>C	XP_011539051.1:p.Gly682Arg
XM_011540750.1:c.1375G>C	XP_011539052.1:p.Gly459Arg
XM_011540748.3:c.2047G>C	XP_011539050.1:p.Gly683Arg
XM_017000370.1:c.2047G>C	XP_016855859.1:p.Gly683Arg
NM_000760.4:c.2041-75G>C MANE Select	NP_000751.1:n.2041-75G>C
NM_172313.3:c.2041-75G>C	NP_758519.1:n.2041-75G>C