Canonical Allele Identifier: CA447156449

Gene: CSF1R

Linked Data

• MyVariant Identifiers: chr5:g.149436883T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150057320T>C , CM000667.2:g.150057320T>C	GRCh38
NC_000005.9:g.149436883T>C , CM000667.1:g.149436883T>C	GRCh37
NC_000005.8:g.149417076T>C	NCBI36
NG_012303.1:g.61053A>G
NG_012303.2:g.61053A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675795.1:c.2286A>G MANE Select	ENSP00000501699.1:p.Val762=
ENST00000286301.7:c.2286A>G	ENSP00000286301.3:p.Val762=
ENST00000504875.5:c.*107A>G	ENSP00000422212.1:n.*107A>G
ENST00000515068.1:c.455A>G	ENSP00000427545.1:n.455A>G
NM_001288705.1:c.2286A>G	NP_001275634.1:p.Val762=
NM_005211.3:c.2286A>G	NP_005202.2:p.Val762=
NR_109969.1:n.2336A>G
NM_001288705.2:c.2286A>G	NP_001275634.1:p.Val762=
NM_001349736.1:c.2286A>G	NP_001336665.1:p.Val762=
NM_001288705.3:c.2286A>G MANE Select	NP_001275634.1:p.Val762=
NM_001375320.1:c.2286A>G	NP_001362249.1:p.Val762=
NM_001375321.1:c.1842A>G	NP_001362250.1:p.Val614=
NR_164679.1:n.2179A>G
NM_001349736.2:c.2286A>G	NP_001336665.1:p.Val762=
NM_005211.4:c.2286A>G	NP_005202.2:p.Val762=
NR_109969.2:n.2250A>G