Canonical Allele Identifier: CA361713725
Community Standard Title: NM_001288705.3(CSF1R):c.1969+1G>A
Gene: CSF1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150060861C>T , CM000667.2:g.150060861C>T GRCh38
NC_000005.9:g.149440424C>T , CM000667.1:g.149440424C>T GRCh37
NC_000005.8:g.149420617C>T NCBI36
NG_012303.1:g.57512G>A
NG_012303.2:g.57512G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001288705.3:c.1969+1G>A MANE Select NP_001275634.1:n.1969+1G>A
ENST00000675795.1:c.1969+1G>A MANE Select ENSP00000501699.1:n.1969+1G>A
NM_001288705.1:c.1969+1G>A NP_001275634.1:n.1969+1G>A
NM_001288705.2:c.1969+1G>A NP_001275634.1:n.1969+1G>A
NM_001349736.1:c.1969+1G>A NP_001336665.1:n.1969+1G>A
NM_001349736.2:c.1969+1G>A NP_001336665.1:n.1969+1G>A
NM_001375320.1:c.1969+1G>A NP_001362249.1:n.1969+1G>A
NM_001375321.1:c.1525+1G>A NP_001362250.1:n.1525+1G>A
NM_005211.3:c.1969+1G>A NP_005202.2:n.1969+1G>A
NM_005211.4:c.1969+1G>A NP_005202.2:n.1969+1G>A
NR_109969.1:n.2182+1G>A
NR_109969.2:n.2096+1G>A
NR_164679.1:n.2025+1G>A
ENST00000286301.7:c.1969+1G>A ENSP00000286301.3:n.1969+1G>A
ENST00000504875.5:c.1969+1G>A ENSP00000422212.1:n.1969+1G>A
ENST00000513609.1:n.626+1G>A
ENST00000515068.1:c.184+1G>A ENSP00000427545.1:n.184+1G>A
ENST00000515239.5:n.499+1G>A