Canonical Allele Identifier: CA2675956547

Gene: CSF1R

Linked Data

• gnomAD v4: 5-150073597-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150073598del , CM000667.2:g.150073598del	GRCh38
NC_000005.9:g.149453161del , CM000667.1:g.149453161del	GRCh37
NC_000005.8:g.149433354del	NCBI36
NG_012303.1:g.44775del
NG_012303.2:g.44775del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675795.1:c.890-105del MANE Select	ENSP00000501699.1:n.890-105del
ENST00000286301.7:c.890-105del	ENSP00000286301.3:n.890-105del
ENST00000504875.5:c.890-105del	ENSP00000422212.1:n.890-105del
ENST00000543093.1:c.890-3027del	ENSP00000445282.1:n.890-3027del
NM_001288705.1:c.890-105del	NP_001275634.1:n.890-105del
NM_005211.3:c.890-105del	NP_005202.2:n.890-105del
NR_109969.1:n.1103-105del
NM_001288705.2:c.890-105del	NP_001275634.1:n.890-105del
NM_001349736.1:c.890-105del	NP_001336665.1:n.890-105del
NM_001288705.3:c.890-105del MANE Select	NP_001275634.1:n.890-105del
NM_001375320.1:c.890-105del	NP_001362249.1:n.890-105del
NM_001375321.1:c.446-105del	NP_001362250.1:n.446-105del
NR_164679.1:n.946-105del
NM_001349736.2:c.890-105del	NP_001336665.1:n.890-105del
NM_005211.4:c.890-105del	NP_005202.2:n.890-105del
NR_109969.2:n.1017-105del