Canonical Allele Identifier: CA447144903

Gene: CSF1R

Linked Data

• MyVariant Identifiers: chr5:g.149452959T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150073396T>A , CM000667.2:g.150073396T>A	GRCh38
NC_000005.9:g.149452959T>A , CM000667.1:g.149452959T>A	GRCh37
NC_000005.8:g.149433152T>A	NCBI36
NG_012303.1:g.44977A>T
NG_012303.2:g.44977A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000675795.1:c.987A>T MANE Select	ENSP00000501699.1:p.Pro329=
ENST00000286301.7:c.987A>T	ENSP00000286301.3:p.Pro329=
ENST00000504875.5:c.987A>T	ENSP00000422212.1:p.Pro329=
ENST00000543093.1:c.890-2825A>T	ENSP00000445282.1:n.890-2825A>T
NM_001288705.1:c.987A>T	NP_001275634.1:p.Pro329=
NM_005211.3:c.987A>T	NP_005202.2:p.Pro329=
NR_109969.1:n.1200A>T
NM_001288705.2:c.987A>T	NP_001275634.1:p.Pro329=
NM_001349736.1:c.987A>T	NP_001336665.1:p.Pro329=
NM_001288705.3:c.987A>T MANE Select	NP_001275634.1:p.Pro329=
NM_001375320.1:c.987A>T	NP_001362249.1:p.Pro329=
NM_001375321.1:c.543A>T	NP_001362250.1:p.Pro181=
NR_164679.1:n.1043A>T
NM_001349736.2:c.987A>T	NP_001336665.1:p.Pro329=
NM_005211.4:c.987A>T	NP_005202.2:p.Pro329=
NR_109969.2:n.1114A>T