Canonical Allele Identifier: CA2675956408
Gene: CSF1R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150073515_150073518del , CM000667.2:g.150073515_150073518del GRCh38
NC_000005.9:g.149453078_149453081del , CM000667.1:g.149453078_149453081del GRCh37
NC_000005.8:g.149433271_149433274del NCBI36
NG_012303.1:g.44855_44858del
NG_012303.2:g.44855_44858del

Transcript Alleles

HGVS Amino-acid Change
ENST00000675795.1:c.890-25_890-22del MANE Select ENSP00000501699.1:n.890-25_890-22del
ENST00000286301.7:c.890-25_890-22del ENSP00000286301.3:n.890-25_890-22del
ENST00000504875.5:c.890-25_890-22del ENSP00000422212.1:n.890-25_890-22del
ENST00000543093.1:c.890-2947_890-2944del ENSP00000445282.1:n.890-2947_890-2944del
NM_001288705.1:c.890-25_890-22del NP_001275634.1:n.890-25_890-22del
NM_005211.3:c.890-25_890-22del NP_005202.2:n.890-25_890-22del
NR_109969.1:n.1103-25_1103-22del
NM_001288705.2:c.890-25_890-22del NP_001275634.1:n.890-25_890-22del
NM_001349736.1:c.890-25_890-22del NP_001336665.1:n.890-25_890-22del
NM_001288705.3:c.890-25_890-22del MANE Select NP_001275634.1:n.890-25_890-22del
NM_001375320.1:c.890-25_890-22del NP_001362249.1:n.890-25_890-22del
NM_001375321.1:c.446-25_446-22del NP_001362250.1:n.446-25_446-22del
NR_164679.1:n.946-25_946-22del
NM_001349736.2:c.890-25_890-22del NP_001336665.1:n.890-25_890-22del
NM_005211.4:c.890-25_890-22del NP_005202.2:n.890-25_890-22del
NR_109969.2:n.1017-25_1017-22del