Canonical Allele Identifier: CA3507205

Gene: CSF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150080328G>A , CM000667.2:g.150080328G>A	GRCh38
NC_000005.9:g.149459891G>A , CM000667.1:g.149459891G>A	GRCh37
NC_000005.8:g.149440084G>A	NCBI36
NG_012303.1:g.38045C>T
NG_012303.2:g.38045C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001288705.3:c.316C>T MANE Select	NP_001275634.1:p.Arg106Trp
ENST00000675795.1:c.316C>T MANE Select	ENSP00000501699.1:p.Arg106Trp
NM_001288705.1:c.316C>T	NP_001275634.1:p.Arg106Trp
NM_001288705.2:c.316C>T	NP_001275634.1:p.Arg106Trp
NM_001349736.1:c.316C>T	NP_001336665.1:p.Arg106Trp
NM_001349736.2:c.316C>T	NP_001336665.1:p.Arg106Trp
NM_001375320.1:c.316C>T	NP_001362249.1:p.Arg106Trp
NM_001375321.1:c.-129C>T	NP_001362250.1:n.-129C>T
NM_005211.3:c.316C>T	NP_005202.2:p.Arg106Trp
NM_005211.4:c.316C>T	NP_005202.2:p.Arg106Trp
NR_109969.1:n.529C>T
NR_109969.2:n.443C>T
NR_164679.1:n.372C>T
ENST00000286301.7:c.316C>T	ENSP00000286301.3:p.Arg106Trp
ENST00000502660.5:n.443C>T
ENST00000504875.5:c.316C>T	ENSP00000422212.1:p.Arg106Trp
ENST00000511344.1:c.-129C>T	ENSP00000421174.1:n.-129C>T
ENST00000543093.1:c.316C>T	ENSP00000445282.1:p.Arg106Trp