Canonical Allele Identifier: CA2746378758

Gene: FCGR3A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161544969_161544970insCCA , CM000663.2:g.161544969_161544970insCCA	GRCh38
NC_000001.10:g.161514759_161514760insCCA , CM000663.1:g.161514759_161514760insCCA	GRCh37
NC_000001.9:g.159781383_159781384insCCA	NCBI36
NG_009066.1:g.10654_10655insTGG , LRG_60:g.10654_10655insTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367967.8:c.320-12_320-11insTGG	ENSP00000356944.3:n.320-12_320-11insTGG
ENST00000426740.8:c.317-12_317-11insTGG	ENSP00000410180.3:n.317-12_317-11insTGG
ENST00000436743.7:c.320-12_320-11insTGG	ENSP00000416607.1:n.320-12_320-11insTGG
ENST00000442336.2:c.317-12_317-11insTGG	ENSP00000396567.2:n.317-12_317-11insTGG
ENST00000699395.1:c.320-12_320-11insTGG	ENSP00000514356.1:n.320-12_320-11insTGG
ENST00000699396.1:c.320-12_320-11insTGG	ENSP00000514357.1:n.320-12_320-11insTGG
ENST00000699397.1:c.320-12_320-11insTGG	ENSP00000514358.1:n.320-12_320-11insTGG
ENST00000699398.1:c.320-12_320-11insTGG	ENSP00000514359.1:n.320-12_320-11insTGG
ENST00000699399.1:c.269-12_269-11insTGG	ENSP00000514360.1:n.269-12_269-11insTGG
ENST00000699400.1:c.317-12_317-11insTGG	ENSP00000514361.1:n.317-12_317-11insTGG
ENST00000699401.1:c.320-12_320-11insTGG	ENSP00000514362.1:n.320-12_320-11insTGG
ENST00000699402.1:c.317-12_317-11insTGG	ENSP00000514363.1:n.317-12_317-11insTGG
ENST00000699493.1:c.*52-12_*52-11insTGG	ENSP00000514404.1:n.*52-12_*52-11insTGG
ENST00000426740.7:c.317-12_317-11insTGG	ENSP00000410180.3:n.317-12_317-11insTGG
ENST00000436743.6:c.320-12_320-11insTGG	ENSP00000416607.1:n.320-12_320-11insTGG
ENST00000443193.6:c.320-12_320-11insTGG MANE Select	ENSP00000392047.2:n.320-12_320-11insTGG
ENST00000367967.7:c.320-12_320-11insTGG	ENSP00000356944.3:n.320-12_320-11insTGG
ENST00000367969.7:c.428-12_428-11insTGG	ENSP00000356946.3:n.428-12_428-11insTGG
ENST00000426740.5:c.370-12_370-11insTGG
ENST00000436743.5:c.320-12_320-11insTGG	ENSP00000416607.1:n.320-12_320-11insTGG
ENST00000443193.5:c.320-12_320-11insTGG	ENSP00000392047.2:n.320-12_320-11insTGG
NM_000569.6:c.428-12_428-11insTGG	NP_000560.5:n.428-12_428-11insTGG
NM_001127592.1:c.425-12_425-11insTGG	NP_001121064.1:n.425-12_425-11insTGG
NM_001127593.1:c.320-12_320-11insTGG , LRG_60t1:c.320-12_320-11insTGG	NP_001121065.1:n.320-12_320-11insTGG
NM_001127595.1:c.320-12_320-11insTGG	NP_001121067.1:n.320-12_320-11insTGG
NM_001127596.1:c.317-12_317-11insTGG	NP_001121068.1:n.317-12_317-11insTGG
XM_011509293.1:c.428-1771_428-1770insTGG	XP_011507595.1:n.428-1771_428-1770insTGG
NM_000569.7:c.635-12_635-11insTGG	NP_000560.6:n.635-12_635-11insTGG
NM_001127592.2:c.632-12_632-11insTGG	NP_001121064.2:n.632-12_632-11insTGG
NM_001329120.1:c.320-12_320-11insTGG	NP_001316049.1:n.320-12_320-11insTGG
NM_001329122.1:c.635-1771_635-1770insTGG	NP_001316051.1:n.635-1771_635-1770insTGG
XM_024454064.1:c.317-12_317-11insTGG	XP_024309832.1:n.317-12_317-11insTGG
NM_001127595.2:c.320-12_320-11insTGG	NP_001121067.1:n.320-12_320-11insTGG
NM_001127596.2:c.317-12_317-11insTGG	NP_001121068.1:n.317-12_317-11insTGG
NM_000569.8:c.320-12_320-11insTGG MANE Select	NP_000560.7:n.320-12_320-11insTGG
NM_001329120.2:c.320-12_320-11insTGG	NP_001316049.1:n.320-12_320-11insTGG
NM_001386450.1:c.317-12_317-11insTGG	NP_001373379.1:n.317-12_317-11insTGG