Canonical Allele Identifier: CA447156447

Gene: CSF1R

Linked Data

• MyVariant Identifiers: chr5:g.149436880G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150057317G>A , CM000667.2:g.150057317G>A	GRCh38
NC_000005.9:g.149436880G>A , CM000667.1:g.149436880G>A	GRCh37
NC_000005.8:g.149417073G>A	NCBI36
NG_012303.1:g.61056C>T
NG_012303.2:g.61056C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675795.1:c.2289C>T MANE Select	ENSP00000501699.1:p.Ala763=
ENST00000286301.7:c.2289C>T	ENSP00000286301.3:p.Ala763=
ENST00000504875.5:c.*110C>T	ENSP00000422212.1:n.*110C>T
ENST00000515068.1:c.458C>T	ENSP00000427545.1:n.458C>T
NM_001288705.1:c.2289C>T	NP_001275634.1:p.Ala763=
NM_005211.3:c.2289C>T	NP_005202.2:p.Ala763=
NR_109969.1:n.2339C>T
NM_001288705.2:c.2289C>T	NP_001275634.1:p.Ala763=
NM_001349736.1:c.2289C>T	NP_001336665.1:p.Ala763=
NM_001288705.3:c.2289C>T MANE Select	NP_001275634.1:p.Ala763=
NM_001375320.1:c.2289C>T	NP_001362249.1:p.Ala763=
NM_001375321.1:c.1845C>T	NP_001362250.1:p.Ala615=
NR_164679.1:n.2182C>T
NM_001349736.2:c.2289C>T	NP_001336665.1:p.Ala763=
NM_005211.4:c.2289C>T	NP_005202.2:p.Ala763=
NR_109969.2:n.2253C>T