Canonical Allele Identifier: CA1590772386
Gene: CSF1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150056199_150056200delinsCA , CM000667.2:g.150056199_150056200delinsCA GRCh38
NC_000005.9:g.149435762_149435763delinsCA , CM000667.1:g.149435762_149435763delinsCA GRCh37
NC_000005.8:g.149415955_149415956delinsCA NCBI36
NG_012303.1:g.62173_62174delinsTG
NG_012303.2:g.62173_62174delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000675795.1:c.2442+19_2442+20delinsTG MANE Select ENSP00000501699.1:n.2442+19_2442+20delinsTG
ENST00000286301.7:c.2442+19_2442+20delinsTG ENSP00000286301.3:n.2442+19_2442+20delinsTG
ENST00000504875.5:c.*263+19_*263+20delinsTG ENSP00000422212.1:n.*263+19_*263+20delinsTG
ENST00000515068.1:c.611+19_611+20delinsTG ENSP00000427545.1:n.611+19_611+20delinsTG
NM_001288705.1:c.2442+19_2442+20delinsTG NP_001275634.1:n.2442+19_2442+20delinsTG
NM_005211.3:c.2442+19_2442+20delinsTG NP_005202.2:n.2442+19_2442+20delinsTG
NR_109969.1:n.2492+19_2492+20delinsTG
NM_001288705.2:c.2442+19_2442+20delinsTG NP_001275634.1:n.2442+19_2442+20delinsTG
NM_001349736.1:c.2442+19_2442+20delinsTG NP_001336665.1:n.2442+19_2442+20delinsTG
NM_001288705.3:c.2442+19_2442+20delinsTG MANE Select NP_001275634.1:n.2442+19_2442+20delinsTG
NM_001375320.1:c.2442+19_2442+20delinsTG NP_001362249.1:n.2442+19_2442+20delinsTG
NM_001375321.1:c.1998+19_1998+20delinsTG NP_001362250.1:n.1998+19_1998+20delinsTG
NR_164679.1:n.2335+19_2335+20delinsTG
NM_001349736.2:c.2442+19_2442+20delinsTG NP_001336665.1:n.2442+19_2442+20delinsTG
NM_005211.4:c.2442+19_2442+20delinsTG NP_005202.2:n.2442+19_2442+20delinsTG
NR_109969.2:n.2406+19_2406+20delinsTG