Canonical Allele Identifier: CA2692961723
Gene: CSF2RA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.1294041_1294042insGACC , CM000685.2:g.1294041_1294042insGACC GRCh38
NC_000023.10:g.1412934_1412935insGACC , CM000685.1:g.1412934_1412935insGACC GRCh37
NC_000023.9:g.1372934_1372935insGACC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000498153.7:c.647-287_647-286insGACC ENSP00000512483.1:n.647-287_647-286insGACC
ENST00000696230.1:c.*730-287_*730-286insGACC ENSP00000512496.1:n.*730-287_*730-286insGACC
ENST00000381529.9:c.647-287_647-286insGACC MANE Select ENSP00000370940.3:n.647-287_647-286insGACC
ENST00000432318.8:c.647-287_647-286insGACC ENSP00000416437.2:n.647-287_647-286insGACC
ENST00000355432.8:c.647-287_647-286insGACC ENSP00000347606.3:n.647-287_647-286insGACC
ENST00000355805.7:c.646+3532_646+3533insGACC ENSP00000348058.2:n.646+3532_646+3533insGACC
ENST00000381500.6:c.647-287_647-286insGACC ENSP00000370911.1:n.647-287_647-286insGACC
ENST00000381509.8:c.647-287_647-286insGACC ENSP00000370920.3:n.647-287_647-286insGACC
ENST00000381524.8:c.647-287_647-286insGACC ENSP00000370935.3:n.647-287_647-286insGACC
ENST00000381529.8:c.647-287_647-286insGACC ENSP00000370940.3:n.647-287_647-286insGACC
ENST00000412290.6:c.647-287_647-286insGACC ENSP00000410667.1:n.647-287_647-286insGACC
ENST00000417535.7:c.647-287_647-286insGACC ENSP00000394227.2:n.647-287_647-286insGACC
ENST00000432318.7:c.647-287_647-286insGACC ENSP00000416437.2:n.647-287_647-286insGACC
ENST00000475259.6:n.58-287_58-286insGACC
ENST00000486791.6:c.647-287_647-286insGACC ENSP00000436825.1:n.647-287_647-286insGACC
ENST00000493312.6:n.684-287_684-286insGACC
ENST00000494969.7:c.244+6843_244+6844insGACC ENSP00000476684.1:n.244+6843_244+6844insGACC
ENST00000501036.7:c.248-287_248-286insGACC ENSP00000440491.1:n.248-287_248-286insGACC
XM_011546165.1:c.647-287_647-286insGACC XP_011544467.1:n.647-287_647-286insGACC
XM_011546166.1:c.647-287_647-286insGACC XP_011544468.1:n.647-287_647-286insGACC
XM_011546167.1:c.647-287_647-286insGACC XP_011544469.1:n.647-287_647-286insGACC
XM_011546168.1:c.647-287_647-286insGACC XP_011544470.1:n.647-287_647-286insGACC
XM_011546169.1:c.647-287_647-286insGACC XP_011544471.1:n.647-287_647-286insGACC
XM_011546170.1:c.647-287_647-286insGACC XP_011544472.1:n.647-287_647-286insGACC
XM_011546171.1:c.647-287_647-286insGACC XP_011544473.1:n.647-287_647-286insGACC
XM_011546172.1:c.647-287_647-286insGACC XP_011544474.1:n.647-287_647-286insGACC
XM_011546173.1:c.647-287_647-286insGACC XP_011544475.1:n.647-287_647-286insGACC
XM_011546174.1:c.647-287_647-286insGACC XP_011544476.1:n.647-287_647-286insGACC
XM_011546175.1:c.647-287_647-286insGACC XP_011544477.1:n.647-287_647-286insGACC
XM_011546176.1:c.515-287_515-286insGACC XP_011544478.1:n.515-287_515-286insGACC
XM_011546165.3:c.647-287_647-286insGACC XP_011544467.1:n.647-287_647-286insGACC
XM_011546167.2:c.647-287_647-286insGACC XP_011544469.1:n.647-287_647-286insGACC
XM_011546168.2:c.647-287_647-286insGACC XP_011544470.1:n.647-287_647-286insGACC
XM_011546170.3:c.647-287_647-286insGACC XP_011544472.1:n.647-287_647-286insGACC
XM_011546174.3:c.647-287_647-286insGACC XP_011544476.1:n.647-287_647-286insGACC
XM_011546175.2:c.647-287_647-286insGACC XP_011544477.1:n.647-287_647-286insGACC
XM_017029287.1:c.647-287_647-286insGACC XP_016884776.1:n.647-287_647-286insGACC
XM_017029288.1:c.647-287_647-286insGACC XP_016884777.1:n.647-287_647-286insGACC