Canonical Allele Identifier: CA1590777646

Gene: CSF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150070483C= , CM000667.2:g.150070483C=	GRCh38
NC_000005.9:g.149450046C= , CM000667.1:g.149450046C=	GRCh37
NC_000005.8:g.149430239C=	NCBI36
NG_012303.1:g.47890G=
NG_012303.2:g.47890G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000675795.1:c.1171G= MANE Select	ENSP00000501699.1:p.Ala391=
ENST00000286301.7:c.1171G=	ENSP00000286301.3:p.Ala391=
ENST00000504875.5:c.1171G=	ENSP00000422212.1:p.Ala391=
NM_001288705.1:c.1171G=	NP_001275634.1:p.Ala391=
NM_005211.3:c.1171G=	NP_005202.2:p.Ala391=
NR_109969.1:n.1384G=
NM_001288705.2:c.1171G=	NP_001275634.1:p.Ala391=
NM_001349736.1:c.1171G=	NP_001336665.1:p.Ala391=
NM_001288705.3:c.1171G= MANE Select	NP_001275634.1:p.Ala391=
NM_001375320.1:c.1171G=	NP_001362249.1:p.Ala391=
NM_001375321.1:c.727G=	NP_001362250.1:p.Ala243=
NR_164679.1:n.1227G=
NM_001349736.2:c.1171G=	NP_001336665.1:p.Ala391=
NM_005211.4:c.1171G=	NP_005202.2:p.Ala391=
NR_109969.2:n.1298G=