Canonical Allele Identifier: CA361760030

Gene: CSF1R

Linked Data

• MyVariant Identifiers: chr5:g.149436881G>T (hg19) ; chr5:g.150057318G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150057318G>T , CM000667.2:g.150057318G>T	GRCh38
NC_000005.9:g.149436881G>T , CM000667.1:g.149436881G>T	GRCh37
NC_000005.8:g.149417074G>T	NCBI36
NG_012303.1:g.61055C>A
NG_012303.2:g.61055C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675795.1:c.2288C>A MANE Select	ENSP00000501699.1:p.Ala763Asp
ENST00000286301.7:c.2288C>A	ENSP00000286301.3:p.Ala763Asp
ENST00000504875.5:c.*109C>A	ENSP00000422212.1:n.*109C>A
ENST00000515068.1:c.457C>A	ENSP00000427545.1:n.457C>A
NM_001288705.1:c.2288C>A	NP_001275634.1:p.Ala763Asp
NM_005211.3:c.2288C>A	NP_005202.2:p.Ala763Asp
NR_109969.1:n.2338C>A
NM_001288705.2:c.2288C>A	NP_001275634.1:p.Ala763Asp
NM_001349736.1:c.2288C>A	NP_001336665.1:p.Ala763Asp
NM_001288705.3:c.2288C>A MANE Select	NP_001275634.1:p.Ala763Asp
NM_001375320.1:c.2288C>A	NP_001362249.1:p.Ala763Asp
NM_001375321.1:c.1844C>A	NP_001362250.1:p.Ala615Asp
NR_164679.1:n.2181C>A
NM_001349736.2:c.2288C>A	NP_001336665.1:p.Ala763Asp
NM_005211.4:c.2288C>A	NP_005202.2:p.Ala763Asp
NR_109969.2:n.2252C>A