Canonical Allele Identifier: CA1202785196
Gene: FCGR3A HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161544672_161544683delinsTGGGCATTCCAG , CM000663.2:g.161544672_161544683delinsTGGGCATTCCAG GRCh38
NC_000001.10:g.161514462_161514473delinsTGGGCATTCCAG , CM000663.1:g.161514462_161514473delinsTGGGCATTCCAG GRCh37
NC_000001.9:g.159781086_159781097delinsTGGGCATTCCAG NCBI36
NG_009066.1:g.10941_10952delinsCTGGAATGCCCA , LRG_60:g.10941_10952delinsCTGGAATGCCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000367967.8:c.577+18_577+29delinsCTGGAATGCCCA ENSP00000356944.3:n.577+18_577+29delinsCTGGAATGCCCA
ENST00000426740.8:c.574+18_574+29delinsCTGGAATGCCCA ENSP00000410180.3:n.574+18_574+29delinsCTGGAATGCCCA
ENST00000436743.7:c.577+18_577+29delinsCTGGAATGCCCA ENSP00000416607.1:n.577+18_577+29delinsCTGGAATGCCCA
ENST00000699395.1:c.577+18_577+29delinsCTGGAATGCCCA ENSP00000514356.1:n.577+18_577+29delinsCTGGAATGCCCA
ENST00000699396.1:c.577+18_577+29delinsCTGGAATGCCCA ENSP00000514357.1:n.577+18_577+29delinsCTGGAATGCCCA
ENST00000699397.1:c.577+18_577+29delinsCTGGAATGCCCA ENSP00000514358.1:n.577+18_577+29delinsCTGGAATGCCCA
ENST00000699398.1:c.595_606delinsCTGGAATGCCCA ENSP00000514359.1:p.Leu199=
ENST00000699399.1:c.526+18_526+29delinsCTGGAATGCCCA ENSP00000514360.1:n.526+18_526+29delinsCTGGAATGCCCA
ENST00000699400.1:c.574+18_574+29delinsCTGGAATGCCCA ENSP00000514361.1:n.574+18_574+29delinsCTGGAATGCCCA
ENST00000699401.1:c.595_606delinsCTGGAATGCCCA ENSP00000514362.1:p.Leu199=
ENST00000426740.7:c.574+18_574+29delinsCTGGAATGCCCA ENSP00000410180.3:n.574+18_574+29delinsCTGGAATGCCCA
ENST00000436743.6:c.577+18_577+29delinsCTGGAATGCCCA ENSP00000416607.1:n.577+18_577+29delinsCTGGAATGCCCA
ENST00000443193.6:c.577+18_577+29delinsCTGGAATGCCCA MANE Select ENSP00000392047.2:n.577+18_577+29delinsCTGGAATGCCCA
ENST00000367967.7:c.577+18_577+29delinsCTGGAATGCCCA ENSP00000356944.3:n.577+18_577+29delinsCTGGAATGCCCA
ENST00000367969.7:c.685+18_685+29delinsCTGGAATGCCCA ENSP00000356946.3:n.685+18_685+29delinsCTGGAATGCCCA
ENST00000426740.5:c.627+18_627+29delinsCTGGAATGCCCA
ENST00000436743.5:c.577+18_577+29delinsCTGGAATGCCCA ENSP00000416607.1:n.577+18_577+29delinsCTGGAATGCCCA
ENST00000443193.5:c.577+18_577+29delinsCTGGAATGCCCA ENSP00000392047.2:n.577+18_577+29delinsCTGGAATGCCCA
NM_000569.6:c.685+18_685+29delinsCTGGAATGCCCA NP_000560.5:n.685+18_685+29delinsCTGGAATGCCCA
NM_001127592.1:c.682+18_682+29delinsCTGGAATGCCCA NP_001121064.1:n.682+18_682+29delinsCTGGAATGCCCA
NM_001127593.1:c.577+18_577+29delinsCTGGAATGCCCA , LRG_60t1:c.577+18_577+29delinsCTGGAATGCCCA NP_001121065.1:n.577+18_577+29delinsCTGGAATGCCCA
NM_001127595.1:c.577+18_577+29delinsCTGGAATGCCCA NP_001121067.1:n.577+18_577+29delinsCTGGAATGCCCA
NM_001127596.1:c.574+18_574+29delinsCTGGAATGCCCA NP_001121068.1:n.574+18_574+29delinsCTGGAATGCCCA
XM_011509293.1:c.428-1484_428-1473delinsCTGGAATGCCCA XP_011507595.1:n.428-1484_428-1473delinsCTGGAATGCCCA
NM_000569.7:c.892+18_892+29delinsCTGGAATGCCCA NP_000560.6:n.892+18_892+29delinsCTGGAATGCCCA
NM_001127592.2:c.889+18_889+29delinsCTGGAATGCCCA NP_001121064.2:n.889+18_889+29delinsCTGGAATGCCCA
NM_001329120.1:c.577+18_577+29delinsCTGGAATGCCCA NP_001316049.1:n.577+18_577+29delinsCTGGAATGCCCA
NM_001329122.1:c.635-1484_635-1473delinsCTGGAATGCCCA NP_001316051.1:n.635-1484_635-1473delinsCTGGAATGCCCA
XM_024454064.1:c.574+18_574+29delinsCTGGAATGCCCA XP_024309832.1:n.574+18_574+29delinsCTGGAATGCCCA
NM_001127595.2:c.577+18_577+29delinsCTGGAATGCCCA NP_001121067.1:n.577+18_577+29delinsCTGGAATGCCCA
NM_001127596.2:c.574+18_574+29delinsCTGGAATGCCCA NP_001121068.1:n.574+18_574+29delinsCTGGAATGCCCA
NM_000569.8:c.577+18_577+29delinsCTGGAATGCCCA MANE Select NP_000560.7:n.577+18_577+29delinsCTGGAATGCCCA
NM_001329120.2:c.577+18_577+29delinsCTGGAATGCCCA NP_001316049.1:n.577+18_577+29delinsCTGGAATGCCCA
NM_001386450.1:c.574+18_574+29delinsCTGGAATGCCCA NP_001373379.1:n.574+18_574+29delinsCTGGAATGCCCA
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