Canonical Allele Identifier: CA913335768

Gene: FCGR3A

Linked Data

• dbSNP Id: rs1557853323
• gnomAD v2: 1-161514307-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161544520_161544521del , CM000663.2:g.161544520_161544521del	GRCh38
NC_000001.10:g.161514310_161514311del , CM000663.1:g.161514310_161514311del	GRCh37
NC_000001.9:g.159780934_159780935del	NCBI36
NG_009066.1:g.11105_11106del , LRG_60:g.11105_11106del

Transcript Alleles

HGVS	Amino-acid change
ENST00000367967.8:c.577+182_577+183del	ENSP00000356944.3:n.577+182_577+183del
ENST00000426740.8:c.574+182_574+183del	ENSP00000410180.3:n.574+182_574+183del
ENST00000436743.7:c.577+182_577+183del	ENSP00000416607.1:n.577+182_577+183del
ENST00000699395.1:c.577+182_577+183del	ENSP00000514356.1:n.577+182_577+183del
ENST00000699396.1:c.577+182_577+183del	ENSP00000514357.1:n.577+182_577+183del
ENST00000699397.1:c.577+182_577+183del	ENSP00000514358.1:n.577+182_577+183del
ENST00000699398.1:c.759_760del	ENSP00000514359.1:p.Cys254PhefsTer8
ENST00000699399.1:c.526+182_526+183del	ENSP00000514360.1:n.526+182_526+183del
ENST00000699400.1:c.574+182_574+183del	ENSP00000514361.1:n.574+182_574+183del
ENST00000699401.1:c.744+15_744+16del	ENSP00000514362.1:n.744+15_744+16del
ENST00000426740.7:c.574+182_574+183del	ENSP00000410180.3:n.574+182_574+183del
ENST00000436743.6:c.577+182_577+183del	ENSP00000416607.1:n.577+182_577+183del
ENST00000443193.6:c.577+182_577+183del MANE Select	ENSP00000392047.2:n.577+182_577+183del
ENST00000367967.7:c.577+182_577+183del	ENSP00000356944.3:n.577+182_577+183del
ENST00000367969.7:c.685+182_685+183del	ENSP00000356946.3:n.685+182_685+183del
ENST00000426740.5:c.627+182_627+183del
ENST00000436743.5:c.577+182_577+183del	ENSP00000416607.1:n.577+182_577+183del
ENST00000443193.5:c.577+182_577+183del	ENSP00000392047.2:n.577+182_577+183del
NM_000569.6:c.685+182_685+183del	NP_000560.5:n.685+182_685+183del
NM_001127592.1:c.682+182_682+183del	NP_001121064.1:n.682+182_682+183del
NM_001127593.1:c.577+182_577+183del , LRG_60t1:c.577+182_577+183del	NP_001121065.1:n.577+182_577+183del
NM_001127595.1:c.577+182_577+183del	NP_001121067.1:n.577+182_577+183del
NM_001127596.1:c.574+182_574+183del	NP_001121068.1:n.574+182_574+183del
XM_011509293.1:c.428-1320_428-1319del	XP_011507595.1:n.428-1320_428-1319del
NM_000569.7:c.892+182_892+183del	NP_000560.6:n.892+182_892+183del
NM_001127592.2:c.889+182_889+183del	NP_001121064.2:n.889+182_889+183del
NM_001329120.1:c.577+182_577+183del	NP_001316049.1:n.577+182_577+183del
NM_001329122.1:c.635-1320_635-1319del	NP_001316051.1:n.635-1320_635-1319del
XM_024454064.1:c.574+182_574+183del	XP_024309832.1:n.574+182_574+183del
NM_001127595.2:c.577+182_577+183del	NP_001121067.1:n.577+182_577+183del
NM_001127596.2:c.574+182_574+183del	NP_001121068.1:n.574+182_574+183del
NM_000569.8:c.577+182_577+183del MANE Select	NP_000560.7:n.577+182_577+183del
NM_001329120.2:c.577+182_577+183del	NP_001316049.1:n.577+182_577+183del
NM_001386450.1:c.574+182_574+183del	NP_001373379.1:n.574+182_574+183del