Canonical Allele Identifier: CA361725373

Gene: CSF1R

Linked Data

• dbSNP Id: rs1758118936
• MyVariant Identifiers: chr5:g.149453046G>T (hg19) ; chr5:g.150073483G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150073483G>T , CM000667.2:g.150073483G>T	GRCh38
NC_000005.9:g.149453046G>T , CM000667.1:g.149453046G>T	GRCh37
NC_000005.8:g.149433239G>T	NCBI36
NG_012303.1:g.44890C>A
NG_012303.2:g.44890C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000675795.1:c.900C>A MANE Select	ENSP00000501699.1:p.Tyr300Ter
ENST00000286301.7:c.900C>A	ENSP00000286301.3:p.Tyr300Ter
ENST00000504875.5:c.900C>A	ENSP00000422212.1:p.Tyr300Ter
ENST00000543093.1:c.890-2912C>A	ENSP00000445282.1:n.890-2912C>A
NM_001288705.1:c.900C>A	NP_001275634.1:p.Tyr300Ter
NM_005211.3:c.900C>A	NP_005202.2:p.Tyr300Ter
NR_109969.1:n.1113C>A
NM_001288705.2:c.900C>A	NP_001275634.1:p.Tyr300Ter
NM_001349736.1:c.900C>A	NP_001336665.1:p.Tyr300Ter
NM_001288705.3:c.900C>A MANE Select	NP_001275634.1:p.Tyr300Ter
NM_001375320.1:c.900C>A	NP_001362249.1:p.Tyr300Ter
NM_001375321.1:c.456C>A	NP_001362250.1:p.Tyr152Ter
NR_164679.1:n.956C>A
NM_001349736.2:c.900C>A	NP_001336665.1:p.Tyr300Ter
NM_005211.4:c.900C>A	NP_005202.2:p.Tyr300Ter
NR_109969.2:n.1027C>A