Canonical Allele Identifier: CA916324627
Gene: FCGR3A HGNC NCBI

Linked Data

dbSNP Id: rs1557853740

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161544818del , CM000663.2:g.161544818del GRCh38
NC_000001.10:g.161514608del , CM000663.1:g.161514608del GRCh37
NC_000001.9:g.159781232del NCBI36
NG_009066.1:g.10807del , LRG_60:g.10807del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367967.8:c.461del ENSP00000356944.3:p.Asn154IlefsTer?
ENST00000426740.8:c.458del ENSP00000410180.3:p.Asn153IlefsTer?
ENST00000436743.7:c.461del ENSP00000416607.1:p.Asn154IlefsTer?
ENST00000699395.1:c.461del ENSP00000514356.1:p.Asn154IlefsTer?
ENST00000699396.1:c.461del ENSP00000514357.1:p.Asn154IlefsTer?
ENST00000699397.1:c.461del ENSP00000514358.1:p.Asn154IlefsTer?
ENST00000699398.1:c.461del ENSP00000514359.1:p.Asn154IlefsTer?
ENST00000699399.1:c.410del ENSP00000514360.1:p.Asn137IlefsTer?
ENST00000699400.1:c.458del ENSP00000514361.1:p.Asn153IlefsTer?
ENST00000699401.1:c.461del ENSP00000514362.1:p.Asn154IlefsTer?
ENST00000699402.1:c.458del ENSP00000514363.1:p.Asn153IlefsTer?
ENST00000426740.7:c.458del ENSP00000410180.3:p.Asn153IlefsTer?
ENST00000436743.6:c.461del ENSP00000416607.1:p.Asn154IlefsTer?
ENST00000443193.6:c.461del MANE Select ENSP00000392047.2:p.Asn154IlefsTer?
ENST00000367967.7:c.461del ENSP00000356944.3:p.Asn154IlefsTer?
ENST00000367969.7:c.569del ENSP00000356946.3:p.Asn190IlefsTer?
ENST00000426740.5:c.511del
ENST00000436743.5:c.461del ENSP00000416607.1:p.Asn154IlefsTer?
ENST00000443193.5:c.461del ENSP00000392047.2:p.Asn154IlefsTer?
NM_000569.6:c.569del NP_000560.5:p.Asn190IlefsTer?
NM_001127592.1:c.566del NP_001121064.1:p.Asn189IlefsTer?
NM_001127593.1:c.461del , LRG_60t1:c.461del NP_001121065.1:p.Asn154IlefsTer?
NM_001127595.1:c.461del NP_001121067.1:p.Asn154IlefsTer?
NM_001127596.1:c.458del NP_001121068.1:p.Asn153IlefsTer?
XM_011509293.1:c.428-1618del XP_011507595.1:n.428-1618del
NM_000569.7:c.776del NP_000560.6:p.Asn259IlefsTer?
NM_001127592.2:c.773del NP_001121064.2:p.Asn258IlefsTer?
NM_001329120.1:c.461del NP_001316049.1:p.Asn154IlefsTer?
NM_001329122.1:c.635-1618del NP_001316051.1:n.635-1618del
XM_024454064.1:c.458del XP_024309832.1:p.Asn153IlefsTer?
NM_001127595.2:c.461del NP_001121067.1:p.Asn154IlefsTer?
NM_001127596.2:c.458del NP_001121068.1:p.Asn153IlefsTer?
NM_000569.8:c.461del MANE Select NP_000560.7:p.Asn154IlefsTer?
NM_001329120.2:c.461del NP_001316049.1:p.Asn154IlefsTer?
NM_001386450.1:c.458del NP_001373379.1:p.Asn153IlefsTer?