Canonical Allele Identifier: CA2537115081

Gene: FCGR3A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161545157_161545158insTTTTT , CM000663.2:g.161545157_161545158insTTTTT	GRCh38
NC_000001.10:g.161514947_161514948insTTTTT , CM000663.1:g.161514947_161514948insTTTTT	GRCh37
NC_000001.9:g.159781571_159781572insTTTTT	NCBI36
NG_009066.1:g.10466_10467insAAAAA , LRG_60:g.10466_10467insAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367967.8:c.320-200_320-199insAAAAA	ENSP00000356944.3:n.320-200_320-199insAAAAA
ENST00000426740.8:c.317-200_317-199insAAAAA	ENSP00000410180.3:n.317-200_317-199insAAAAA
ENST00000436743.7:c.320-200_320-199insAAAAA	ENSP00000416607.1:n.320-200_320-199insAAAAA
ENST00000442336.2:c.317-200_317-199insAAAAA	ENSP00000396567.2:n.317-200_317-199insAAAAA
ENST00000699395.1:c.320-200_320-199insAAAAA	ENSP00000514356.1:n.320-200_320-199insAAAAA
ENST00000699396.1:c.320-200_320-199insAAAAA	ENSP00000514357.1:n.320-200_320-199insAAAAA
ENST00000699397.1:c.320-200_320-199insAAAAA	ENSP00000514358.1:n.320-200_320-199insAAAAA
ENST00000699398.1:c.320-200_320-199insAAAAA	ENSP00000514359.1:n.320-200_320-199insAAAAA
ENST00000699399.1:c.269-200_269-199insAAAAA	ENSP00000514360.1:n.269-200_269-199insAAAAA
ENST00000699400.1:c.317-200_317-199insAAAAA	ENSP00000514361.1:n.317-200_317-199insAAAAA
ENST00000699401.1:c.320-200_320-199insAAAAA	ENSP00000514362.1:n.320-200_320-199insAAAAA
ENST00000699402.1:c.317-200_317-199insAAAAA	ENSP00000514363.1:n.317-200_317-199insAAAAA
ENST00000699493.1:c.*52-200_*52-199insAAAAA	ENSP00000514404.1:n.*52-200_*52-199insAAAAA
ENST00000426740.7:c.317-200_317-199insAAAAA	ENSP00000410180.3:n.317-200_317-199insAAAAA
ENST00000436743.6:c.320-200_320-199insAAAAA	ENSP00000416607.1:n.320-200_320-199insAAAAA
ENST00000443193.6:c.320-200_320-199insAAAAA MANE Select	ENSP00000392047.2:n.320-200_320-199insAAAAA
ENST00000367967.7:c.320-200_320-199insAAAAA	ENSP00000356944.3:n.320-200_320-199insAAAAA
ENST00000367969.7:c.428-200_428-199insAAAAA	ENSP00000356946.3:n.428-200_428-199insAAAAA
ENST00000426740.5:c.370-200_370-199insAAAAA
ENST00000436743.5:c.320-200_320-199insAAAAA	ENSP00000416607.1:n.320-200_320-199insAAAAA
ENST00000443193.5:c.320-200_320-199insAAAAA	ENSP00000392047.2:n.320-200_320-199insAAAAA
NM_000569.6:c.428-200_428-199insAAAAA	NP_000560.5:n.428-200_428-199insAAAAA
NM_001127592.1:c.425-200_425-199insAAAAA	NP_001121064.1:n.425-200_425-199insAAAAA
NM_001127593.1:c.320-200_320-199insAAAAA , LRG_60t1:c.320-200_320-199insAAAAA	NP_001121065.1:n.320-200_320-199insAAAAA
NM_001127595.1:c.320-200_320-199insAAAAA	NP_001121067.1:n.320-200_320-199insAAAAA
NM_001127596.1:c.317-200_317-199insAAAAA	NP_001121068.1:n.317-200_317-199insAAAAA
XM_011509293.1:c.428-1959_428-1958insAAAAA	XP_011507595.1:n.428-1959_428-1958insAAAAA
NM_000569.7:c.635-200_635-199insAAAAA	NP_000560.6:n.635-200_635-199insAAAAA
NM_001127592.2:c.632-200_632-199insAAAAA	NP_001121064.2:n.632-200_632-199insAAAAA
NM_001329120.1:c.320-200_320-199insAAAAA	NP_001316049.1:n.320-200_320-199insAAAAA
NM_001329122.1:c.635-1959_635-1958insAAAAA	NP_001316051.1:n.635-1959_635-1958insAAAAA
XM_024454064.1:c.317-200_317-199insAAAAA	XP_024309832.1:n.317-200_317-199insAAAAA
NM_001127595.2:c.320-200_320-199insAAAAA	NP_001121067.1:n.320-200_320-199insAAAAA
NM_001127596.2:c.317-200_317-199insAAAAA	NP_001121068.1:n.317-200_317-199insAAAAA
NM_000569.8:c.320-200_320-199insAAAAA MANE Select	NP_000560.7:n.320-200_320-199insAAAAA
NM_001329120.2:c.320-200_320-199insAAAAA	NP_001316049.1:n.320-200_320-199insAAAAA
NM_001386450.1:c.317-200_317-199insAAAAA	NP_001373379.1:n.317-200_317-199insAAAAA