Canonical Allele Identifier: CA2675956683

Gene: CSF1R

Linked Data

• gnomAD v4: 5-150070403-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150070405dup , CM000667.2:g.150070405dup	GRCh38
NC_000005.9:g.149449968dup , CM000667.1:g.149449968dup	GRCh37
NC_000005.8:g.149430161dup	NCBI36
NG_012303.1:g.47969dup
NG_012303.2:g.47969dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675795.1:c.1198+52dup MANE Select	ENSP00000501699.1:n.1198+52dup
ENST00000286301.7:c.1198+52dup	ENSP00000286301.3:n.1198+52dup
ENST00000504875.5:c.1198+52dup	ENSP00000422212.1:n.1198+52dup
NM_001288705.1:c.1198+52dup	NP_001275634.1:n.1198+52dup
NM_005211.3:c.1198+52dup	NP_005202.2:n.1198+52dup
NR_109969.1:n.1411+52dup
NM_001288705.2:c.1198+52dup	NP_001275634.1:n.1198+52dup
NM_001349736.1:c.1198+52dup	NP_001336665.1:n.1198+52dup
NM_001288705.3:c.1198+52dup MANE Select	NP_001275634.1:n.1198+52dup
NM_001375320.1:c.1198+52dup	NP_001362249.1:n.1198+52dup
NM_001375321.1:c.754+52dup	NP_001362250.1:n.754+52dup
NR_164679.1:n.1254+52dup
NM_001349736.2:c.1198+52dup	NP_001336665.1:n.1198+52dup
NM_005211.4:c.1198+52dup	NP_005202.2:n.1198+52dup
NR_109969.2:n.1325+52dup