Canonical Allele Identifier: CA361721964

Gene: CSF1R

Linked Data

• gnomAD v4: 5-150070485-C-A
• MyVariant Identifiers: chr5:g.149450048C>A (hg19) ; chr5:g.150070485C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150070485C>A , CM000667.2:g.150070485C>A	GRCh38
NC_000005.9:g.149450048C>A , CM000667.1:g.149450048C>A	GRCh37
NC_000005.8:g.149430241C>A	NCBI36
NG_012303.1:g.47888G>T
NG_012303.2:g.47888G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675795.1:c.1169G>T MANE Select	ENSP00000501699.1:p.Arg390Ile
ENST00000286301.7:c.1169G>T	ENSP00000286301.3:p.Arg390Ile
ENST00000504875.5:c.1169G>T	ENSP00000422212.1:p.Arg390Ile
NM_001288705.1:c.1169G>T	NP_001275634.1:p.Arg390Ile
NM_005211.3:c.1169G>T	NP_005202.2:p.Arg390Ile
NR_109969.1:n.1382G>T
NM_001288705.2:c.1169G>T	NP_001275634.1:p.Arg390Ile
NM_001349736.1:c.1169G>T	NP_001336665.1:p.Arg390Ile
NM_001288705.3:c.1169G>T MANE Select	NP_001275634.1:p.Arg390Ile
NM_001375320.1:c.1169G>T	NP_001362249.1:p.Arg390Ile
NM_001375321.1:c.725G>T	NP_001362250.1:p.Arg242Ile
NR_164679.1:n.1225G>T
NM_001349736.2:c.1169G>T	NP_001336665.1:p.Arg390Ile
NM_005211.4:c.1169G>T	NP_005202.2:p.Arg390Ile
NR_109969.2:n.1296G>T