Canonical Allele Identifier: CA1590779897

Gene: CSF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150073819_150073821delinsAAC , CM000667.2:g.150073819_150073821delinsAAC	GRCh38
NC_000005.9:g.149453382_149453384delinsAAC , CM000667.1:g.149453382_149453384delinsAAC	GRCh37
NC_000005.8:g.149433575_149433577delinsAAC	NCBI36
NG_012303.1:g.44552_44554delinsGTT
NG_012303.2:g.44552_44554delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675795.1:c.890-328_890-326delinsGTT MANE Select	ENSP00000501699.1:n.890-328_890-326delinsGTT
ENST00000286301.7:c.890-328_890-326delinsGTT	ENSP00000286301.3:n.890-328_890-326delinsGTT
ENST00000504875.5:c.890-328_890-326delinsGTT	ENSP00000422212.1:n.890-328_890-326delinsGTT
ENST00000543093.1:c.890-3250_890-3248delinsGTT	ENSP00000445282.1:n.890-3250_890-3248delinsGTT
NM_001288705.1:c.890-328_890-326delinsGTT	NP_001275634.1:n.890-328_890-326delinsGTT
NM_005211.3:c.890-328_890-326delinsGTT	NP_005202.2:n.890-328_890-326delinsGTT
NR_109969.1:n.1103-328_1103-326delinsGTT
NM_001288705.2:c.890-328_890-326delinsGTT	NP_001275634.1:n.890-328_890-326delinsGTT
NM_001349736.1:c.890-328_890-326delinsGTT	NP_001336665.1:n.890-328_890-326delinsGTT
NM_001288705.3:c.890-328_890-326delinsGTT MANE Select	NP_001275634.1:n.890-328_890-326delinsGTT
NM_001375320.1:c.890-328_890-326delinsGTT	NP_001362249.1:n.890-328_890-326delinsGTT
NM_001375321.1:c.446-328_446-326delinsGTT	NP_001362250.1:n.446-328_446-326delinsGTT
NR_164679.1:n.946-328_946-326delinsGTT
NM_001349736.2:c.890-328_890-326delinsGTT	NP_001336665.1:n.890-328_890-326delinsGTT
NM_005211.4:c.890-328_890-326delinsGTT	NP_005202.2:n.890-328_890-326delinsGTT
NR_109969.2:n.1017-328_1017-326delinsGTT