Canonical Allele Identifier: CA1590772387

Gene: CSF1R

Linked Data

• dbSNP Id: rs1757211776

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150056201del , CM000667.2:g.150056201del	GRCh38
NC_000005.9:g.149435764del , CM000667.1:g.149435764del	GRCh37
NC_000005.8:g.149415957del	NCBI36
NG_012303.1:g.62173del
NG_012303.2:g.62173del

Transcript Alleles

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