Canonical Allele Identifier: CA361724568
Gene: CSF1R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150073373G>T , CM000667.2:g.150073373G>T GRCh38
NC_000005.9:g.149452936G>T , CM000667.1:g.149452936G>T GRCh37
NC_000005.8:g.149433129G>T NCBI36
NG_012303.1:g.45000C>A
NG_012303.2:g.45000C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000675795.1:c.1010C>A MANE Select ENSP00000501699.1:p.Thr337Asn
ENST00000286301.7:c.1010C>A ENSP00000286301.3:p.Thr337Asn
ENST00000504875.5:c.1010C>A ENSP00000422212.1:p.Thr337Asn
ENST00000543093.1:c.890-2802C>A ENSP00000445282.1:n.890-2802C>A
NM_001288705.1:c.1010C>A NP_001275634.1:p.Thr337Asn
NM_005211.3:c.1010C>A NP_005202.2:p.Thr337Asn
NR_109969.1:n.1223C>A
NM_001288705.2:c.1010C>A NP_001275634.1:p.Thr337Asn
NM_001349736.1:c.1010C>A NP_001336665.1:p.Thr337Asn
NM_001288705.3:c.1010C>A MANE Select NP_001275634.1:p.Thr337Asn
NM_001375320.1:c.1010C>A NP_001362249.1:p.Thr337Asn
NM_001375321.1:c.566C>A NP_001362250.1:p.Thr189Asn
NR_164679.1:n.1066C>A
NM_001349736.2:c.1010C>A NP_001336665.1:p.Thr337Asn
NM_005211.4:c.1010C>A NP_005202.2:p.Thr337Asn
NR_109969.2:n.1137C>A