Canonical Allele Identifier: CA361724691

Gene: CSF1R

Linked Data

• MyVariant Identifiers: chr5:g.149452960G>T (hg19) ; chr5:g.150073397G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150073397G>T , CM000667.2:g.150073397G>T	GRCh38
NC_000005.9:g.149452960G>T , CM000667.1:g.149452960G>T	GRCh37
NC_000005.8:g.149433153G>T	NCBI36
NG_012303.1:g.44976C>A
NG_012303.2:g.44976C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000675795.1:c.986C>A MANE Select	ENSP00000501699.1:p.Pro329Gln
ENST00000286301.7:c.986C>A	ENSP00000286301.3:p.Pro329Gln
ENST00000504875.5:c.986C>A	ENSP00000422212.1:p.Pro329Gln
ENST00000543093.1:c.890-2826C>A	ENSP00000445282.1:n.890-2826C>A
NM_001288705.1:c.986C>A	NP_001275634.1:p.Pro329Gln
NM_005211.3:c.986C>A	NP_005202.2:p.Pro329Gln
NR_109969.1:n.1199C>A
NM_001288705.2:c.986C>A	NP_001275634.1:p.Pro329Gln
NM_001349736.1:c.986C>A	NP_001336665.1:p.Pro329Gln
NM_001288705.3:c.986C>A MANE Select	NP_001275634.1:p.Pro329Gln
NM_001375320.1:c.986C>A	NP_001362249.1:p.Pro329Gln
NM_001375321.1:c.542C>A	NP_001362250.1:p.Pro181Gln
NR_164679.1:n.1042C>A
NM_001349736.2:c.986C>A	NP_001336665.1:p.Pro329Gln
NM_005211.4:c.986C>A	NP_005202.2:p.Pro329Gln
NR_109969.2:n.1113C>A