Canonical Allele Identifier: CA1590779743

Gene: CSF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150073438C= , CM000667.2:g.150073438C=	GRCh38
NC_000005.9:g.149453001C= , CM000667.1:g.149453001C=	GRCh37
NC_000005.8:g.149433194C=	NCBI36
NG_012303.1:g.44935G=
NG_012303.2:g.44935G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675795.1:c.945G= MANE Select	ENSP00000501699.1:p.Val315=
ENST00000286301.7:c.945G=	ENSP00000286301.3:p.Val315=
ENST00000504875.5:c.945G=	ENSP00000422212.1:p.Val315=
ENST00000543093.1:c.890-2867G=	ENSP00000445282.1:n.890-2867G=
NM_001288705.1:c.945G=	NP_001275634.1:p.Val315=
NM_005211.3:c.945G=	NP_005202.2:p.Val315=
NR_109969.1:n.1158G=
NM_001288705.2:c.945G=	NP_001275634.1:p.Val315=
NM_001349736.1:c.945G=	NP_001336665.1:p.Val315=
NM_001288705.3:c.945G= MANE Select	NP_001275634.1:p.Val315=
NM_001375320.1:c.945G=	NP_001362249.1:p.Val315=
NM_001375321.1:c.501G=	NP_001362250.1:p.Val167=
NR_164679.1:n.1001G=
NM_001349736.2:c.945G=	NP_001336665.1:p.Val315=
NM_005211.4:c.945G=	NP_005202.2:p.Val315=
NR_109969.2:n.1072G=