Canonical Allele Identifier: CA447144918

Gene: CSF1R

Linked Data

• MyVariant Identifiers: chr5:g.149452977G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150073414G>C , CM000667.2:g.150073414G>C	GRCh38
NC_000005.9:g.149452977G>C , CM000667.1:g.149452977G>C	GRCh37
NC_000005.8:g.149433170G>C	NCBI36
NG_012303.1:g.44959C>G
NG_012303.2:g.44959C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675795.1:c.969C>G MANE Select	ENSP00000501699.1:p.Val323=
ENST00000286301.7:c.969C>G	ENSP00000286301.3:p.Val323=
ENST00000504875.5:c.969C>G	ENSP00000422212.1:p.Val323=
ENST00000543093.1:c.890-2843C>G	ENSP00000445282.1:n.890-2843C>G
NM_001288705.1:c.969C>G	NP_001275634.1:p.Val323=
NM_005211.3:c.969C>G	NP_005202.2:p.Val323=
NR_109969.1:n.1182C>G
NM_001288705.2:c.969C>G	NP_001275634.1:p.Val323=
NM_001349736.1:c.969C>G	NP_001336665.1:p.Val323=
NM_001288705.3:c.969C>G MANE Select	NP_001275634.1:p.Val323=
NM_001375320.1:c.969C>G	NP_001362249.1:p.Val323=
NM_001375321.1:c.525C>G	NP_001362250.1:p.Val175=
NR_164679.1:n.1025C>G
NM_001349736.2:c.969C>G	NP_001336665.1:p.Val323=
NM_005211.4:c.969C>G	NP_005202.2:p.Val323=
NR_109969.2:n.1096C>G