Canonical Allele Identifier: CA447144832

Gene: CSF1R

Linked Data

• MyVariant Identifiers: chr5:g.149452905A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150073342A>C , CM000667.2:g.150073342A>C	GRCh38
NC_000005.9:g.149452905A>C , CM000667.1:g.149452905A>C	GRCh37
NC_000005.8:g.149433098A>C	NCBI36
NG_012303.1:g.45031T>G
NG_012303.2:g.45031T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675795.1:c.1041T>G MANE Select	ENSP00000501699.1:p.Pro347=
ENST00000286301.7:c.1041T>G	ENSP00000286301.3:p.Pro347=
ENST00000504875.5:c.1041T>G	ENSP00000422212.1:p.Pro347=
ENST00000543093.1:c.890-2771T>G	ENSP00000445282.1:n.890-2771T>G
NM_001288705.1:c.1041T>G	NP_001275634.1:p.Pro347=
NM_005211.3:c.1041T>G	NP_005202.2:p.Pro347=
NR_109969.1:n.1254T>G
NM_001288705.2:c.1041T>G	NP_001275634.1:p.Pro347=
NM_001349736.1:c.1041T>G	NP_001336665.1:p.Pro347=
NM_001288705.3:c.1041T>G MANE Select	NP_001275634.1:p.Pro347=
NM_001375320.1:c.1041T>G	NP_001362249.1:p.Pro347=
NM_001375321.1:c.597T>G	NP_001362250.1:p.Pro199=
NR_164679.1:n.1097T>G
NM_001349736.2:c.1041T>G	NP_001336665.1:p.Pro347=
NM_005211.4:c.1041T>G	NP_005202.2:p.Pro347=
NR_109969.2:n.1168T>G