Canonical Allele Identifier: CA1590777677

Gene: CSF1R

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150066358T>G , CM000667.2:g.150066358T>G	GRCh38
NC_000005.9:g.149445921T>G , CM000667.1:g.149445921T>G	GRCh37
NC_000005.8:g.149426114T>G	NCBI36
NG_012303.1:g.52015A>C
NG_012303.2:g.52015A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675795.1:c.1626+1857A>C MANE Select	ENSP00000501699.1:n.1626+1857A>C
ENST00000286301.7:c.1626+1857A>C	ENSP00000286301.3:n.1626+1857A>C
ENST00000504875.5:c.1626+1857A>C	ENSP00000422212.1:n.1626+1857A>C
ENST00000513609.1:n.156+668A>C
ENST00000515239.5:n.156+668A>C
NM_001288705.1:c.1626+1857A>C	NP_001275634.1:n.1626+1857A>C
NM_005211.3:c.1626+1857A>C	NP_005202.2:n.1626+1857A>C
NR_109969.1:n.1839+1857A>C
NM_001288705.2:c.1626+1857A>C	NP_001275634.1:n.1626+1857A>C
NM_001349736.1:c.1626+1857A>C	NP_001336665.1:n.1626+1857A>C
NM_001288705.3:c.1626+1857A>C MANE Select	NP_001275634.1:n.1626+1857A>C
NM_001375320.1:c.1626+1857A>C	NP_001362249.1:n.1626+1857A>C
NM_001375321.1:c.1182+1857A>C	NP_001362250.1:n.1182+1857A>C
NR_164679.1:n.1682+1857A>C
NM_001349736.2:c.1626+1857A>C	NP_001336665.1:n.1626+1857A>C
NM_005211.4:c.1626+1857A>C	NP_005202.2:n.1626+1857A>C
NR_109969.2:n.1753+1857A>C