Canonical Allele Identifier: CA1202785226

Gene: FCGR3A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161544760_161544761delinsCT , CM000663.2:g.161544760_161544761delinsCT	GRCh38
NC_000001.10:g.161514550_161514551delinsCT , CM000663.1:g.161514550_161514551delinsCT	GRCh37
NC_000001.9:g.159781174_159781175delinsCT	NCBI36
NG_009066.1:g.10863_10864delinsAG , LRG_60:g.10863_10864delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367967.8:c.517_518delinsAG	ENSP00000356944.3:p.Arg173=
ENST00000426740.8:c.514_515delinsAG	ENSP00000410180.3:p.Arg172=
ENST00000436743.7:c.517_518delinsAG	ENSP00000416607.1:p.Arg173=
ENST00000699395.1:c.517_518delinsAG	ENSP00000514356.1:p.Arg173=
ENST00000699396.1:c.517_518delinsAG	ENSP00000514357.1:p.Arg173=
ENST00000699397.1:c.517_518delinsAG	ENSP00000514358.1:p.Arg173=
ENST00000699398.1:c.517_518delinsAG	ENSP00000514359.1:p.Arg173=
ENST00000699399.1:c.466_467delinsAG	ENSP00000514360.1:p.Arg156=
ENST00000699400.1:c.514_515delinsAG	ENSP00000514361.1:p.Arg172=
ENST00000699401.1:c.517_518delinsAG	ENSP00000514362.1:p.Arg173=
ENST00000426740.7:c.514_515delinsAG	ENSP00000410180.3:p.Arg172=
ENST00000436743.6:c.517_518delinsAG	ENSP00000416607.1:p.Arg173=
ENST00000443193.6:c.517_518delinsAG MANE Select	ENSP00000392047.2:p.Arg173=
ENST00000367967.7:c.517_518delinsAG	ENSP00000356944.3:p.Arg173=
ENST00000367969.7:c.625_626delinsAG	ENSP00000356946.3:p.Arg209=
ENST00000426740.5:c.567_568delinsAG
ENST00000436743.5:c.517_518delinsAG	ENSP00000416607.1:p.Arg173=
ENST00000443193.5:c.517_518delinsAG	ENSP00000392047.2:p.Arg173=
NM_000569.6:c.625_626delinsAG	NP_000560.5:p.Arg209=
NM_001127592.1:c.622_623delinsAG	NP_001121064.1:p.Arg208=
NM_001127593.1:c.517_518delinsAG , LRG_60t1:c.517_518delinsAG	NP_001121065.1:p.Arg173=
NM_001127595.1:c.517_518delinsAG	NP_001121067.1:p.Arg173=
NM_001127596.1:c.514_515delinsAG	NP_001121068.1:p.Arg172=
XM_011509293.1:c.428-1562_428-1561delinsAG	XP_011507595.1:n.428-1562_428-1561delinsAG
NM_000569.7:c.832_833delinsAG	NP_000560.6:p.Arg278=
NM_001127592.2:c.829_830delinsAG	NP_001121064.2:p.Arg277=
NM_001329120.1:c.517_518delinsAG	NP_001316049.1:p.Arg173=
NM_001329122.1:c.635-1562_635-1561delinsAG	NP_001316051.1:n.635-1562_635-1561delinsAG
XM_024454064.1:c.514_515delinsAG	XP_024309832.1:p.Arg172=
NM_001127595.2:c.517_518delinsAG	NP_001121067.1:p.Arg173=
NM_001127596.2:c.514_515delinsAG	NP_001121068.1:p.Arg172=
NM_000569.8:c.517_518delinsAG MANE Select	NP_000560.7:p.Arg173=
NM_001329120.2:c.517_518delinsAG	NP_001316049.1:p.Arg173=
NM_001386450.1:c.514_515delinsAG	NP_001373379.1:p.Arg172=