Canonical Allele Identifier: CA1590777624
Gene: CSF1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150070462G= , CM000667.2:g.150070462G= GRCh38
NC_000005.9:g.149450025G= , CM000667.1:g.149450025G= GRCh37
NC_000005.8:g.149430218G= NCBI36
NG_012303.1:g.47911C=
NG_012303.2:g.47911C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000675795.1:c.1192C= MANE Select ENSP00000501699.1:p.Leu398=
ENST00000286301.7:c.1192C= ENSP00000286301.3:p.Leu398=
ENST00000504875.5:c.1192C= ENSP00000422212.1:p.Leu398=
NM_001288705.1:c.1192C= NP_001275634.1:p.Leu398=
NM_005211.3:c.1192C= NP_005202.2:p.Leu398=
NR_109969.1:n.1405C=
NM_001288705.2:c.1192C= NP_001275634.1:p.Leu398=
NM_001349736.1:c.1192C= NP_001336665.1:p.Leu398=
NM_001288705.3:c.1192C= MANE Select NP_001275634.1:p.Leu398=
NM_001375320.1:c.1192C= NP_001362249.1:p.Leu398=
NM_001375321.1:c.748C= NP_001362250.1:p.Leu250=
NR_164679.1:n.1248C=
NM_001349736.2:c.1192C= NP_001336665.1:p.Leu398=
NM_005211.4:c.1192C= NP_005202.2:p.Leu398=
NR_109969.2:n.1319C=