Canonical Allele Identifier: CA361721868

Gene: CSF1R

Linked Data

• gnomAD v4: 5-150070468-G-T
• COSMIC: COSM4384032 ; COSM4384033
• MyVariant Identifiers: chr5:g.149450031G>T (hg19) ; chr5:g.150070468G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150070468G>T , CM000667.2:g.150070468G>T	GRCh38
NC_000005.9:g.149450031G>T , CM000667.1:g.149450031G>T	GRCh37
NC_000005.8:g.149430224G>T	NCBI36
NG_012303.1:g.47905C>A
NG_012303.2:g.47905C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675795.1:c.1186C>A MANE Select	ENSP00000501699.1:p.Leu396Ile
ENST00000286301.7:c.1186C>A	ENSP00000286301.3:p.Leu396Ile
ENST00000504875.5:c.1186C>A	ENSP00000422212.1:p.Leu396Ile
NM_001288705.1:c.1186C>A	NP_001275634.1:p.Leu396Ile
NM_005211.3:c.1186C>A	NP_005202.2:p.Leu396Ile
NR_109969.1:n.1399C>A
NM_001288705.2:c.1186C>A	NP_001275634.1:p.Leu396Ile
NM_001349736.1:c.1186C>A	NP_001336665.1:p.Leu396Ile
NM_001288705.3:c.1186C>A MANE Select	NP_001275634.1:p.Leu396Ile
NM_001375320.1:c.1186C>A	NP_001362249.1:p.Leu396Ile
NM_001375321.1:c.742C>A	NP_001362250.1:p.Leu248Ile
NR_164679.1:n.1242C>A
NM_001349736.2:c.1186C>A	NP_001336665.1:p.Leu396Ile
NM_005211.4:c.1186C>A	NP_005202.2:p.Leu396Ile
NR_109969.2:n.1313C>A